A systematic framework for understanding the microbiome in human health and disease: from basic principles to clinical translation

The human microbiome is a complex and dynamic system that plays important roles in human health and disease. However, there remain limitations and theoretical gaps in our current understanding of the intricate relationship between microbes and humans. In this narrative review, we integrate the knowledge and insights from various fields, including anatomy, physiology, immunology, histology, genetics, and evolution, to propose a systematic framework. It introduces key concepts such as the ‘innate and adaptive genomes’, which enhance genetic and evolutionary comprehension of the human genome. The ‘germ-free syndrome’ challenges the traditional ‘microbes as pathogens’ view, advocating for the necessity of microbes for health. The ‘slave tissue’ concept underscores the symbiotic intricacies between human tissues and their microbial counterparts, highlighting the dynamic health implications of microbial interactions. ‘Acquired microbial immunity’ positions the microbiome as an adjunct to human immune systems, providing a rationale for probiotic therapies and prudent antibiotic use. The ‘homeostatic reprogramming hypothesis’ integrates the microbiome into the internal environment theory, potentially explaining the change in homeostatic indicators post-industrialization. The ‘cell-microbe co-ecology model’ elucidates the symbiotic regulation affecting cellular balance, while the ‘meta-host model’ broadens the host definition to include symbiotic microbes. The ‘health-illness conversion model’ encapsulates the innate and adaptive genomes’ interplay and dysbiosis patterns. The aim here is to provide a more focused and coherent understanding of microbiome and highlight future research avenues that could lead to a more effective and efficient healthcare system.


INTRODUCTION
8][9] In symbiosis with the human body, the microbiome -a collective of microbes such as bacteria, fungi, archaea, viruses and their respective genomes, maintains a continuous crosstalk with the human genome.Exploring their interplay may elucidate a broader spectrum of individual phenotypic variations, considering that genomic differences between individuals account for only 0.1% of the total genome. 10icroorganisms were first discovered and reported by Antoni van Leeuwenhoek in the 17 th century using microscope. 11dvancements in modern techniques such as high-throughput sequencing, multi-OMICS, and artificial intelligence have greatly facilitated our understanding of the value of human microbiomes in health and disease.Notably, the Human Microbiome Project (HMP) and Integrative Human Microbiome Project (iHMP), [12][13][14][15] European MetaHIT project (Metagenomics of the Human Intestinal Tract), [16][17][18][19][20] American Gut Project (AGP), 21 Dutch Microbiome Project (DMP) 22 are prominent studies in this field.7][28][29][30][31][32][33][34][35][36][37][38][39][40][41][42][43] Also, some conceptual terms have significantly enhanced our understanding of the human-microbe relationship.5][46] The "hologenome" frames the human genome and the genetic content of microbiomes as a single entity. 47The characterization of microbial physiological functions led us to consider them as another "organ". 480][51] Despite their insightful contributions, the fragmented nature and limitations (will be discussed in the main text) of these hypotheses or theories have impeded a unified understanding of the microbiome.
To establish a systematic understanding of the role of the microbiome in human health and disease, this review first delves into the anatomical distribution and characteristics of the microbiome within the human body, elucidating its regulatory mechanisms on physiological functions.Among them, we introduce the concept of "acquired microbe immunity," which synthesizes the microbiome's "colonization resistance" and "immune modulation" functions.By further examining the physiological traits of germ-free animals, the complete knockout of microbial genomes, we termed "germ-free syndrome".The abnormalities resulting from the loss of the microbiome further prompt us to explore the integrity of the human genome parts through the lens of genetics and evolution.Herein, the "adaptive genome" refers to the external and dynamic microbiome, while the "innate genome" denotes the inherent genetic blueprint that humans are born with.The introduction of the "adaptive genome" concept allows us to extend the notion of a single host to that of a "meta-host", thereby gaining a comprehensive understanding of disease heterogeneity or the success rate of organ transplantation resulting from hostmicrobiome interactions.To address the complex interplay of physiological dependence and conflict with microbes, the hypothesis of "slave tissue" was introduced, viewing the microbe as an exogenous tissue under the control of human master tissues such as nerve, connective, epithelial and muscle tissues.Recognizing that homeostasis theory is fundamental to understanding health and disease, we further discuss the hypothesis of "homeostasis reprogramming" based on the theoretical foundation of the adaptive genome and slave tissue.Utilizing the "cell-microbe co-ecology model," we describe the phenomenon of co-homeostasis between microbes and human cells.Lastly, to deepen our understanding of how microbes contribute to disease, a "health-disease conversion model" was proposed, outlining the common patterns of dysbiosis.To conclude, the above envisioned coherent and systematic conceptual framework is expected to bolster the effectiveness and efficiency of the healthcare system.

HUMAN MICROBIAL DISTRIBUTION, DEVELOPMENT, PERSONALIZATION, AND STABILIZATION
The human body is inhabited by diverse microorganisms including bacteria, fungi, archaea and viruses (bacteriophages).Throughout long human history, microorganisms have co-evolved with us, [52][53][54][55][56][57][58][59][60][61] exhibiting periodic variations that align with the different stages of a person's life. 37These microbes are mainly found in the mucosal and superficial layers of organs and can interact with the environment.Of the known bacterial distributions, the gastrointestinal tract is the most densely populated (29%), followed by the oral cavity (26%) and skin (21%), while the respiratory tract (14%) and urogenital tract (9%) have lower densities 62 (Fig. 1).Microbial communities also show density gradients within specific organs, such as higher densities in the upper respiratory tract than in the lower respiratory tract, and lower densities in the stomach, duodenum, and jejunum than in the ileum and colon. 62erging insights in traditionally sterile human sites Anatomical sites traditionally considered sterile in human anatomy are now being challenged by the emergence or potential existence of resident microbiota, albeit with some controversy.The environment on diseased blood vessels is non-sterile, containing bacteria and viruses, with the sequencing of arterial atherosclerosis providing compelling evidence. 63Alison Clifford et al. extensively discussed the presence of normal vascular microbiota, but the evidence is largely from non-viable samples. 64sing strict exclusion criteria, aseptic sampling, repeated measures, and negative controls to eliminate potential contamination, László Hidi et al. analyzed microbiomes in femoral arteries from brain-dead donors, mainly those with hemorrhagic or ischemic strokes. 65They identified Proteobacteria, Firmicutes, and Actinobacteria as the predominant phyla, with Staphylococcus, Pseudomonas, Corynebacterium, Bacillus, Acinetobacter, and Propionibacterium being prevalent genera. 65Additionally, they observed a notable correlation between blood type and microbiota diversity. 65Although limitations such as the small sample size (14 participants) and the older age range of donors (40-60  years) reduce the power of this study and the lack of characterization of microbial function, 65 it however provides valuable insights into the possible presence of the microbiome in the normal human vasculature and potential research directions for unraveling vasculature-based diseases.Interestingly however, despite previous findings of approximately 1% of the human body's bacterial presence in blood samples from the Human Microbiome Project, an analysis of 9770 samples from healthy individuals revealed the absence of similar microbial communities in the bloodstream. 62,66Notably, 82% of the sampled population exhibited no microbial sequences, emphasizing the sterile nature of the blood in healthy individuals. 668][69][70] Similarly, the brain has long been considered a sterile organ because of its blood-brain barrier and immunity. 71However, surprising findings from the microscopic examination of multiple brain regions post-mortem in healthy individuals, presented at a neuroscience conference, have revealed the existence of microbiota in the brain. 72Nevertheless, convincing evidence awaits confirmation using animal models and independent human material. 73Certain organs responsible for the secretion of body fluids also contain microbiota.For Fig. 1 Human microbial-related characteristics.The distribution data of the microbiome were obtained from the Human Microbiome Project, 62,657 supplemented by modified data from Ron Sender et al. 658,659 example, although sampling difficulties exist, a study on healthy humans confirmed the presence of microbial community in the gallbladder which may retrograde entry of gastrointestinal microbiota. 74In women aged 18-90, a diverse range of bacteria, predominantly belonging to Proteobacteria, have been identified in mammary tissue. 757][78][79][80][81] A recent comprehensive discussion suggests that the detected microbes may be due to contamination, emphasizing the lack of reliable evidence for the presence of microbial colonization. 82lonization and development of common microbiomes Although microbial sampling can't cover every anatomical niche or the complete microbiome, including bacteria, viruses, and fungi, throughout an individual's entire lifespan, microbiome composition is influenced by various factors like host and environmental factors (which will be discussed in the section on adaptive genome), substantial progress has been made in recent decades in sequencing the microbiomes of the gut, oral cavity, skin, vagina, and lung.Overall, microbiota development initiates at birth, with the primary succession phase characterized by rapid microbial changes that decelerate into a more stable "climax community" by adolescence. 83This community, while relatively stable, can still experience fluctuations in adulthood. 37Disturbances such as antibiotics or infections may prompt secondary succession, potentially leading to a new microbial state. 84Finally, in old age, the microbiota undergoes final succession, typically resulting in a community with reduced diversity. 37Below, we will provide a brief overview of the microbiota throughout the lifespan by integrating current knowledge.While much of the information has been comprehensively reviewed, 37,85,86 we include some of the latest research findings.

Digestive tract microbiome
In the early stages, newborns acquire pioneer microorganisms from their mother's vaginal tract, skin and possibly through fecal exposure during the birth process.The gut bacteria are initially dominated by Bifidobacterium spp.and gradually shifts to a mixed community of Bifidobacterium, Clostridium and Bacteroides spp.by the end of the first year. 87This shift is accompanied by a greater diversity of genera within the Firmicutes, including Clostridia, Faecalibacterium, Ruminococcus and Veillonella, while the abundance of Bifidobacterium spp.decreases. 15At approximately 3 years of age, the gut microbiota stabilizes and is dominated by Firmicutes and Bacteroidetes. 88However, the majority of the studies to date are largely based on easily accessible fecal samples, and endoscopic examinations are also limited by singlesite sampling in certain areas. 80To study the distribution of microbiota across multiple regions of the human intestinal tract under undisturbed and uncontaminated conditions, in 2023, Dari Shalon et al. developed an ingestible capsule device capable of sampling four specific sites from the small intestine to the ascending colon suggesting that specific microbial phyla may be enriched in specific intestinal segments compared to fecal samples. 89,90A more detailed and rigorous identification was conducted by Jun-Jun She et al. who sampled seven surface organs of deceased individuals within 1.5 h postmortem. 91In their study, Helicobacter species were found to be enriched in the esophagus and can also be found in the stomach, where it likely contributes to the fatty acid metabolism alongside Lactobacillus. 91revotella, which accumulates in the duodenum, is potentially involved in the degradation of carbohydrates and amino acid synthesis. 91Enterococcus and Bacteroides are enriched in the ileum, where they may play a role in amino acid synthesis and the enterohepatic circulation of bile acids. 91Lastly, the right colon is characterized by an enrichment of Klebsiella, Enterococcus and Lactobacillus, which are likely engaged in fermentation processes and the production of short-chain fatty acids, while the left colon shows an enrichment of Parabacteroides, Bifidobacterium and Dorea, indicating their involvement in intestinal motility and bile acid metabolism. 91Of note, the biogeographical map also emphasizes the presence of bacterial translocation along the upper and lower gastrointestinal tract due to luminal flow conditions, as well as significant differences between mucosal and luminal samples. 91In general, the microbial diversity in the esophagus and stomach is markedly lower compared to the small intestine and colon. 91

Oral microbiome
The oral bacterial community is initially dominated by the genera Streptococcus, Gemella, Granulicatella, and Veillonella at birth, followed by an increase in Lactobacillus and Fusobacterium. 92taphylococcus reaches its peak around 3 months of age before declining, making way for an increase in Gemella, Granulicatella, Haemophilus, and Rothia species. 93][96] Interestingly, re-analysis of raw 16S rRNA sequences of over 2000 saliva samples from 47 different studies identified 68 consistent core bacterial taxa. 97Streptococcus oralis subspecies dentisani is recognized as a potentially beneficial organism for oral health and is highly abundant across different oral niches in healthy humans. 97The Neisseria genus, dominant in the salivary microbiome, is associated with lipid metabolism pathways, suggesting a key role in regulating oral lipid-related metabolic processes. 97Lautropia, in conjunction with Neisseria, has been found to increase the abundance of certain metabolic pathways in Chinese samples, particularly those involved in lipid metabolism. 97n contrast, the Prevotella genus, which is less abundant in Western populations, may be linked to a reduction in specific metabolic pathways when compared to Chinese samples. 97The Veillonella genus, which is more abundant in Western populations, is linked to the 'Flavone and flavonol biosynthesis' pathway, whereas the Atopobium genus is observed to be less prevalent in the same demographic. 97

Skin microbiome
The skin bacterial community initially has a high presence of maternal vaginal Lactobacillus spp. at birth. 83By around weeks 4-5, the infant skin microbiota starts resembling that of adults but becomes more specific to different body areas during adolescence. 98Common genera include Staphylococcus and Corynebacterium, with Pseudomonas, Enterobacter, Enterococcus, Proteus, and Klebsiella at specific sites like the armpit or forearm. 99The skin bacteria can primarily be categorized into three major classes: sebaceous or oily including the face, chest, and back; moist such as the bend of the elbow, back of the knee, and groin; and dry like the volar forearm and palm.Sebaceous skin regions are notably enriched with Propionibacterium acnes and exhibit a variety of metabolic pathways that are pivotal to lipid metabolism and energy production, including glycolysis, ATP and GTP generation, and NADH dehydrogenase I. 100,101 In contrast, dry skin regions are characterized by a distinct microbial composition that includes species such as Corynebacterium and Staphylococcus epidermidis, with a significant enrichment in citrate cycle modules that are likely adapted to the drier conditions of these areas. 100,102Moist skin regions are predominantly inhabited by fungi, particularly Malassezia globosa and Malassezia restricta, which thrive in the higher-humidity environment. 100,103The toenail region, which is unique compared to other skin types, houses a specific microbial community that is distinguished by its energy production components, including the conversion of oxaloacetate to fructose-6-phosphate, and the presence of ATPase and ATP synthase. 100Additionally, the skin's microbiome as a whole serves as a reservoir for antibiotic resistance genes, displaying considerable variability among individuals and resistance types, with certain classes like MATE efflux pumps being highly hostspecific. 100,103ginal microbiome Dominated by a single Lactobacillus species, the human vaginal microbiome is intriguingly different from that of other species, including primates. 104Currently, with a lack of reliable data on the neonatal vaginal microbiota, the developmental trajectory of the human vaginal microbiome remains incompletely understood.Before puberty, the vaginal microbiome exhibits high diversity, including streptococci, enterococci and anaerobes, possibly due to the thinning of vaginal epithelial cells and minimal glycogen deposition resulting from lower estrogen levels, which may not provide sufficient nutrition for Lactobacilli. 105However, in premenopausal women, the vaginal microbiome is dominated by one or a few Lactobacillus species, such as L. crispatus, L. iners, L. jensenii or L. gasseri, leading to reduced microbial diversity. 106This dominance is accompanied by an increase in oestrogen levels. 1068][109] Although approximately 25% of North American women have vaginal microbiomes that are not dominated by Lactobacilli, but instead consist of a mixture of anaerobic and aerobic bacteria, such as Gardnerella, Prevotella, Atopobium, Sneathia, Megasphaera and Peptoniphilus. 1102][113][114][115][116] A recent notable study called "Isala", conducted in Belgium, involved selfsampling (using citizen science methods) of 3,345 women. 117n this cohort of healthy individuals, L. crispatus was the most common taxonomic unit (43.2%), followed by L. iners (27.7%) and G. vaginalis (9.8%). 118spiratory microbiome Encompassing the nasal cavity, sinuses, pharynx and supraglottic portion of the larynx, the upper respiratory tract has different microbial compositions in different regions. 119In particular, the nasal cavity and nasopharynx are dominated by Moraxella, Staphylococcus, Corynebacterium, Haemophilus and Streptococcus species, whereas the oropharynx hosts Prevotella, Veillonella, Streptococcus, Leptotrichia, Rothia, Neisseria and Haemophilus species. 120In neonates, the lower respiratory tract microbial community is dominated by either Staphylococcus or Ureaplasma species during the first weeks of life, correlating with mode of delivery; vaginal births enrich for Ureaplasma, whereas cesarean births enrich for Staphylococcus. 121In the first 2 postnatal months, lung microbiome diversifies to include oral commensals such as Streptococcus, Prevotella, Porphyromonas and Veillonella. 121However, the lower respiratory tract, comprising the trachea and lungs, maintain a low biomass that is essential for efficient gas exchange, supported by a rapid clearance system including immune actions such as mucociliary clearance and phagocytic activity of macrophages, as well as mechanisms like pulmonary surfactant and cough reflex. 122,123rsonalization and relative stability The abundance and composition of microbial communities in different anatomical ecological niches can be influenced and disturbed by multiple host and external factors, resulting in highly personalized variations. 1246][127] In a recent contribution from the iHMP, Zhou et al. reported on the dynamics of microbiomes at three body sites-oral, nasal, and skin-and in fecal samples from 86 individuals monitored longitudinally over six years. 128Their findings highlight the variable stability of the human microbiome across different individuals and anatomical sites, with fecal and oral microbiomes showing greater stability than those from the skin and nasal microbes. 128Moreover, microbiome characterized by high individual specificity are more stable over time, reflecting an enhanced regulation by the host. 128Microbes closely associated with human development can also serve as means to predict chronological age, with the skin microbiome offering the most accurate age predictions (mean error ± standard deviation of 3.8 ± 0.45 years), outperforming both the oral microbiome (4.5 ± 0.14 years) and the gut microbiome (11.5 ± 0.12 years). 129n summary, in reviewing the past deciphering efforts, we are progressing along the path of identifying common microbiota, then core microbiota, and finally individualized microbiota.At the same time, the accompanying exploration of microbiota functionality and perturbation mechanisms is approaching the possibility of regulation.

PHYSIOLOGY AND REGULATORY ROLE OF COMMENSAL MICROBES
Digestion and microbiome-related products Microbiome-related products encompass a range of substances, including microbiota-derived metabolites (MDM), microbiotaderived components (MDC), and microbiota-secreted proteins (MSP). 130Nestled in the complex ecosystem of the digestive tract, a thriving microbial community produces an extensive repertoire of metabolic enzymes (biogenic enzymes, glycosidases, and proteases), thereby enhancing the digestive and metabolic capabilities of the human body. 15,16For example, humans lack specific and efficient nitrate reductases 131 which is essential to convert dietary nitrate into nitrite and Nitric oxide (NO) through the nitrate-nitrite-NO pathway. 132The oral cavity harbors nitratereducing bacteria, such as Veillonella and Actinomyces. 133The nitrate reductase Nar in oral bacteria is encoded by genes narX, narG, narJ, narH, narY, narI, and narW. 134Additionally, certain bacteria like Rothia possess nitrite reductase encoded by genes nirK and nirS, which further reduce nitrite to NO. 135 NO has long been recognized as an endothelium-derived relaxing factor, functioning as a vasodilator and modulating vascular tone, blood pressure, and hemodynamics. 136,137nvolved in the synthesis of vitamin K and most water-soluble B vitamins, these microorganisms actively contribute to the production of prothrombin and osteocalcin, thus influencing blood coagulation and bone metabolism. 26They also serve as essential cofactors and coenzymes that are central to various cellular metabolic pathways. 138Beyond their enzymatic contributions, gut-dwelling microbes orchestrate the assimilation and conversion of carbohydrates, proteins, and amino acids, yielding a range of essential products. 139,140These include short-chain fatty acids (SCFAs) as well as branched-chain amino acids (BCAAs), secondary bile acids (BAs), polyamines, lipids and an enigmatic realm known as "dark matter". 26,138These remarkable entities have emerged as key participants in human tissue development, neural function, immune response (Fig. 2), metabolism, and behavioral regulation, revealing their profound impact on human well-being. 141It's important to note that the digestive tract serves as the primary gateway for the body to actively absorb nutrients and substances from the external environment.As a result, the oral and gastrointestinal microbiomes play an integral role in digestion.Whereas, microbes in other sites of the body are primarily involved in physiological regulation through mechanisms such as colonization resistance, immune modulation and maternal transmission.

Metabolic regulation
Short-chain fatty acid.Anaerobic bacteria ferment nondigestible substrates such as non-starch polysaccharides, resistant starch, and oligosaccharides, resulting in the production of SCFAs (mainly including acetate, propionate, and butyrate). 142he majority of these SCFAs are rapidly and almost completely absorbed by colon cells. 143Acetate enters the liver through the portal vein and is released into the peripheral tissues for cholesterol metabolism and fatty acid synthesis. 1446][147][148] Butyrate controls intestinal hormones, reduces appetite and food intake. 149Importantly, butyrate metabolism serves as a source of energy for 60-70% of the colon, maintaining a hypoxic state in the gut through β-oxidation, reducing intestinal inflammation and preserving mucosal integrity. 150,151[154] Secondary bile acids.The gut microbiota actively participates in the conversion of primary bile acids to secondary bile acids and plays a crucial role in the enterohepatic circulation of bile acids. 155t exerts regulatory control over glucose homeostasis, lipid metabolism, insulin signaling, and inflammation through the FXR and TGR5 receptors. 156[157] Arg-Lys-His.The novel tripeptide Arg-Lys-His (RKH), synthesized by Akkermansia muciniphila (AKK), binds to TLR4 receptors and inhibits TLR4-mediated signaling pathways.This reduces sepsisinduced inflammatory cell activation and excessive cytokine release which protects against sepsis-related mortality and organ damage. 158dole-3-propionic acid (IPA).IPA was found to be decreased in a mouse model of autism spectrum disorder (ASD) leading to deficits in social interaction and cognitive memory. 159Mechanistically, IPA restores inhibitory synaptic transmission in the hippocampal region by activating the ERK1 signaling pathway, which is encoded by the MAPK3 gene located within the 16p11.2chromosomal region. 159movanillic acid (HVA).Bifidobacterium longum (B.longum) produces HVA, a metabolite that modulates synaptic integrity by inhibiting excessive autophagy. 160This mechanism reduces the degradation of microtubule-associated protein 1 light chain 3 (LC3) and the protein SQSTM1/p62, safeguarding the synaptic vesicle membrane of hippocampal neurons and contributing to depression alleviation. 160Roseburia intestinalis (R. intestinalis), athough not a HVA producer, facilitates the growth of B. longum, indirectly enhancing HVA synthesis. 160lso, the induction of specific Helper T cell 17 (Th17) expression by skin commensal microbiota is associated with transcriptional programs relevant to skin-neuronal interactions and repair. 161ollowing skin injury, Th17 cells upregulate IL-17A, which binds to IL-17A receptors upregulated on damaged nerves, promoting axonal growth and local nerve regeneration. 161Disruption of the Fig. 2 Acquired microbial immunity.The human immune consists of innate and acquired immunity, which is mainly carried out by T and B cells.The main strategies of adaptive immunity are active and passive immunization.In active immunity, natural immunity can be acquired by direct infection with the pathogen, while vaccination with the antigen is the artificial way.Passive immunization is mainly achieved by natural means, such as breastfeeding, or artificial means, such as immunoglobulin injections.Commensal microbiota described here can provide another form of acquired defence and regulating power against pathogens (commensal microbiota immunity).Correspondingly, maternal human milk oligosaccharides (HMOs), acquired through maternal reproductive transmission and exposure, can enhance the colonization of beneficial microbes under natural conditions.Under artificial conditions, fecal microbiota transplantation (FMT), [660][661][662][663][664] probiotics, [665][666][667][668][669] prebiotics, 670 synbiotics 671,672 and postbiotics [673][674][675][676] can be used to acquire this immunity.Commensal microbiota immunity strengthens cellular barriers and regulates immune cells through metabolites such as short-chain fatty acids.They train and educate the immune system as a competitor while providing colonization resistance against foreign and established pathogenic microbes.The decline of commensal microbiota immunity increases the risk of skin and food allergies, 677 asthma, 548 type 1 diabetes (T1D), 678 pathogenic overgrowth (such as Clostridium difficile), 667,[679][680][681][682][683][684][685][686][687] and susceptibility to inflammatory bowel disease (IBD) 555,[688][689][690][691][692][693][694][695] and other potential diseases 696,697 pulmonary microbiota significantly influences susceptibility to autoimmune diseases of the central nervous system. 162Augmenting microbial populations capable of producing lipopolysaccharide (LPS) can enhance endogenous immune factors in brain microglial cells, thus modulating neuroimmune responses in the brain. 162igenetic modulation Epigenetic changes represent reversible modifications in gene expression regulation and heritable traits that occur without permanent changes to the DNA sequence, and can even be transmitted to offspring through sexual reproduction.[163][164][165][166] It has duly been established that the human microbiota can extensively influence the expression of the human genome through mechanisms such as DNA methylation, histone modification, non-coding RNA and chromatin remodeling, leading to a broad range of physiological impacts.167 Early-life epigenetic crosstalk significantly impacts the development of adult tissues.168 DNA methylation. DNA metylation at CpG islands can recruit methyl-CpG-binding proteins, which alter chromatin conformation, leading to chromatin condensation that prevents the binding of transcription factors and RNA polymerase, thus inhibiting the expression of specific genes.169 Metabolites produced by microbial communities can serve as substrates and/or co-factors in these reactions/interactions.For example, folate can metabolically generate S-adenosylmethionine (SAM), which becomes a substrate for DNA and histone methylation.170 Microbiota can adjust DNA methylation in mice intestinal epithelial cells, affecting the expression of 824 upregulated and 358 downregulated genes.168 TET2/3 enzymes are key in this process, facilitating the conversion of 5-methylcytosine to 5-hydroxymethylcytosine, which promotes demethylation and the activation of genes essential for intestinal homeostasis.168 Histone modification.Histones are the fundamental proteins that make up chromatin, tightly binding with DNA to form nucleosome structures, which then coil and fold into complex chromatin. 171Modifications of histones, like acetylation and methylation, regulate the condensation of chromatin, thus regulating gene expression.172 For example, microbiota-derived butyrate can inhibit the activity of histone deacetylases (HDACs), leading to increased acetylation of histone H3 at the Foxp3 gene locus.173 This acetylation enhances the expression of the Foxp3 gene, facilitating the differentiation of colonic regulatory T cells (Treg). 173t microbiota can also regulates intestinal epithelial gene expression by suppressing Hepatocyte Nuclear Factor 4 Alpha (HNF4A) through reduced DNA binding and altered histone modifications such as Histone 3 Lysine 4 monomethylation (H3K4me1) and Histone 3 Lysine 27 acetylation (H3K27ac), which could be linked to the pathogenesis of Inflammatory Bowel Disease (IBD).174 Non-coding RNA.Non-coding RNAs (ncRNAs), including micro-RNAs (miRNAs), circular RNAs (circRNAs) and long non-coding RNAs (lncRNAs), regulate host gene expression through various mechanisms.175 MiRNAs modulate protein synthesis within host cells by binding to complementary sequences on messenger RNAs (mRNAs), leading to mRNA degradation or translational repression, while circRNAs function as "sponges" for miRNAs, sequestering them to modulate their activity.176 Microbiota can influences the expression of the miR-181 in white adipose tissue of mice through the production of tryptophan-derived metabolites, such as indole and indole-3-carboxylic acid (I3CA).177 This mechanism leads to a decrease in miR-181 expression within white adipocytes, which in turn stimulates increased energy expenditure and enhanced insulin sensitivity, counteracting the development of dietinduced obesity and insulin resistance. 177LncRNAs regulate genes through multiple mechanisms: they can organize protein complexes on DNA, direct proteins to gene sites, and change the epigenetic marks that control gene activity.178 They also interact with transcription factors, influence mRNA splicing and produce regulatory RNAs like miRNAs.178 Significant differences in lncRNA expression occur when germ-free mice are re-colonized with distinct microbial types, such as complex mouse microbiota, E. coli or E. coli expressing bile salt hydrolase (EC-BSH), with only a few lncRNAs showing overlap and most being type-specific.179 Immunomodulation Commensal microorganisms play a fundamental role in the education and maintenance of immune homeostasis.In the past few decades, there has been a notable increase in the incidence of allergic diseases, such as asthma, atopic dermatitis, and food allergies, as well as autoimmune diseases like type 1 diabetes (T1D) in industrialized countries.49,180,181 Interestingly, individuals who migrate from countries with low incidence rates of these conditions to those with higher rates, and do so before a certain age threshold, tend to adopt the disease prevalence of their host country.For instance, research indicates that children who move to countries with higher incidences of allergic asthma before the age of 5 are more likely to develop asthma at rates similar to those of the host country's population.182 Similarly, the risk of type 1 diabetes has been observed to increase in migrants who move before adolescence, with studies suggesting a critical age threshold around 15 years for the development of multiple sclerosis.[183][184][185][186] In 1989, David Strachan proposed the novel concept that infections could serve as a preventative measure against the development of allergic diseases. 187Building on this idea, in 2000, he formally introduced the term "hygiene hypothesis" to describe the observed correlation between a lower incidence of infectious diseases in early life and the rising prevalence of allergic conditions, 188 which exerted a profound influence on public health.189,190 Subsequently, Rook et al. as well as Noverr and Huffnagle, further emphasized the "Old Friends Hypothesis" or "Microflora Hypothesis," highlighting the importance of microorganisms in achieving immune homeostasis in the human body.191,192 It is recognized that the immune system development of the individual involves critical developmental periods.193 Early exposure to a diverse range of microbes is essential for the proper development of the immune system, with the activation of immune regulatory pathways, particularly through Toll-like receptors (TLRs), fostering a balanced immune response.This process is thought to promote the generation of regulatory T cells (Treg), which produce anti-inflammatory cytokines like IL-10 and TGF-β, thus suppressing excessive immune reactions and potentially reducing the risk of developing allergic and autoimmune diseases.The protective effects of commensals are also suggested to involve antigenic competition and the modulation of inflammatory responses, possibly through mechanisms like TLR desensitization. 193olonization resistance Microbial communities that inhabit human mucosal surfaces or skin are capable of preventing the colonization of pathogens and overgrowth of indigenous pathogens, known as "colonization resistance" (Fig. 2).194,195 This phenomenon was first discovered by Bohnhoff and Miller in 1967 when they observed increased susceptibility of mice to Salmonella infection following treatment with streptomycin.196 This antibiotic-related susceptibility explains the widespread harm caused by antibiotic abuse in recent years, 197,198 as commensal microbial colonization appears to provide the body with an additional defense mechanism.They compete with pathogens through various mechanisms for the specific nutritional and physicochemical environment of the human body, ultimately leaving newcomers unable to secure adequate nutrition and space for survival and reproduction.199 The way microbes protect their own territory may indirectly protect the human body.For example, S. salivarius TOVE-R strain is effective against virulent streptococci like S. mutans, S. sobrinus and S. pyogenes, which are associated with tooth decay, pharyngitis, and periodontitis.200 Its bacteriocin (a type of heterogenous peptide) inhibits S. pyogenes and S. pneumoniae 200 and can also modulates immune responses by inhibiting inflammatory pathways activated by these pathogens.201 Coagulase-negative staphylococci (CoNS), which are typically present in the skin and nasal cavity, secrete bacteriocins that reduce the colonization of pathogenic S. aureus.202 The commensal bacterium S. epidermidis, through the secretion of serine protease Esp, can degrade and inhibit the biofilm of S. aureus, reducing its virulence. 203rres Salazar et al. have elucidated that S. epidermidis can also produces a novel, rapidly degrading broad-spectrum antibacterial agent termed epifadin, which demonstrates efficacy in mitigating nasal colonization by S. aureus.204 Analyzing 2229 bacterial genomes from the Human Microbiome Project, sourced from diverse body sites such as skin, gastrointestinal tract, urogenital tract, mouth, and trachea, researchers identified gene clusters encoding for lanthipeptides and lasso peptides.205 These clusters direct the synthesis of peptides that, through unique post-translational modifications, give rise to novel compounds exhibiting antimicrobial activity.205 In addition to bacteriocin and enzyme secretion, common metabolites such as SCFAs can inhibit the growth of pathogenic Escherichia coli, 206 Clostridium difficile, 207 and Salmonella 208 in the gut.Moreover, secondary bile acids have been shown to inhibit many Gram-positive bacteria, including C. difficile.209 Nevertheless, microbes can also develop resistance to being colonized by other microbes through direct physical interactions.Contact-dependent inhibition systems have been discovered in microorganisms such as E. coli and Pseudomonas aeruginosa, which can inhibit neighboring microbes by targeting their receptor proteins.210,211 Many Gram-negative bacteria, such as P. aeruginosa and Burkholderia spp., can use type VI secretion systems (T6SS), a multi-protein complex that punctures nearby microbes and injects toxic proteins.[212][213][214][215] Interestingly, microbes that occupy niches also participate in the niche modification. A cmonly cited example is Lactobacilli, a resident of the vaginal microbiota, which lowers the pH of the vagina, thereby reducing the colonization of pathogenic bacteria that can thrive in neutral environment.110,216,217 The mechanisms of microbial colonization resistance may shift depending on the environment where they are situated.In germ-free or antibiotic-treated mice, e.g.Klebsiella oxytoca inhibits the growth of S. Typhimurium by producing toxins such as tilimycin.218 Whereas, in mice with a complex microbiota, K. oxytoca competes with S. Typhimurium for survival resources by utilizing specific carbohydrates like dulcitol.218 In general, if the exposed areas of the human body are inevitably colonized by external microbes, perhaps the best strategy would be to use controlled microbes as the first line of defense in external immunity, thus minimizing the disruption of internal immunity.Salvarsan, the first antibiotic in 1910, heralded a medical revolution. 219The subsequent discovery of penicillin in 1928 propelled us into the golden age of antibiotics, pivotal in saving lives and advancing civilization.220 However, the widespread utilization of antimicrobial drugs has resulted in a rising incidence of infections caused by antimicrobial resistance (AMR) globally, leaving us in a quandary with diminishing treatment alternatives.221 In 2019 alone, an estimated 4.95 million deaths were linked to bacterial AMR, with 1.27 million deaths directly attributable to it.197 By exploiting the immunomodulatory properties of microorganisms and implementing colonization resistance strategies, it is hoped that dependence on antimicrobial drugs will be reduced and a promising path will be opened in the present predicament.

Regulation and transmission of parental microbiota
The maternal gut microbiota produces SCFAs that can enter the embryo through the mother bloodstream. 222SCFAs act on the GPR41 receptor in the sympathetic nervous system of the fetus and GPR43 receptor, which is highly expressed in intestinal epithelial cells and pancreatic beta cells, promoting the development of prenatal metabolic system in neurons, enteroendocrine cells and beta cells. 222This reduces the risk of offspring developing metabolic syndrome. 222The normal development of the fetal brain and nervous system in mice is also influenced by maternal microbiota and its metabolites. 223Treatment with antibiotics or germ-free pregnancy in mice can lead to defective growth of embryonic hypothalamic axon and a decrease in tactile sensitivity in adulthood. 223Although research in humans is limited, a recent follow-up study of 860 children found an association between the maternal gut microbiota during pregnancy and neurodevelopment in the first year after birth. 224In addition, the presence of Clostridia in the maternal gut microbiota is associated with high fine motor skills in children. 224Microbial colonization also drives innate immune development in offspring, increasing certain innate lymphocytes and monocytes while causing widespread changes in the gene expression profile of the intestinal epithelial mucosa, better preparation for colonization by postnatal microbes and prevention of microbial invasion. 225In conclusion, maternal microbiota during pregnancy may participate in the regulation of fetal endocrine, neural and immune development through multiple mechanisms.However, vaginal and fecal contact, as well as skin-to-skin contact and later breastfeeding, provide more than half of the initial microbial colonization for infants. 226While the transmissibility of different microbial species can vary depending on the mode and place of delivery, species such as Bifidobacterium have demonstrated consistent vertical transmission regardless of the delivery environment. 227In addition to supporting the development of vital organs 228 and providing defense against harmful bacteria in the infant's gut, 229,230 maternal milk provides probiotics 231 and human milk oligosaccharides (HMOs) that facilitate the metabolism and colonization of beneficial bacteria like Bifidobacterium. 2326][237][238] Fathers are also a consistent source of infant strains and their cumulative contribution equals that of mothers after one year. 239Recent research suggests that dysbiosis in the gut microbiota of male mice prior to conception can affect testicular function and sperm quality, as well as lead to compromised placental function in female mice, thereby increasing the risk of offspring with low birth weight, severe growth restriction and early mortality. 240These findings underscore the potential value of microbiota in guiding reproductive health.

GERM-FREE SYNDROME
David, also known as the "Bubble Boy", was born in 1971 with severe combined immune deficiency syndrome (SCID) and lived his entire life in a sterile isolation unit. 241Unfortunately, he died at the age of 12 years due to severe infection. 241Although it was rarest of the cases, due to the lack of advanced technologies available today, incomprehensive health evaluations, particularly the lack of anatomical data, prevent us from fully understanding this unique germ-free human individual.More importantly, individuals with underlying diseases are also not an ideal subject for research.3][244][245] The progressive commercialization of GF mice/rat in laboratories has elucidated the phenotypes of these animals, shedding light on the intricate interplay between the microbiome and the health of organisms.

Systemic somatic growth and development
At the age of 8 weeks, GF mice exhibited a 14.5% reduction in weight and were 4% shorter in stature compared to their conventionally raised (CONV-R) peers. 246The disparity in weight was not a result of increased adiposity, as both groups demonstrated equivalent adipose tissue and serum leptin levels. 246After weaning, GF mice consumed food at a rate comparable to their body weight as CONV-R mice did, yet differences in nutrient absorption and utilization efficiency may account for growth discrepancies. 246Despite elevated early levels of growth hormone in GF mice, this did not enhance insulin-like growth factor-1 (IGF-1) and insulin-like growth factor binding protein 3 (IGFBP-3) levels, indicating growth hormone resistance. 246Most organs and tissues, including the heart, liver, spleen, thymus, thyroid, skin and intestine, are reduced in mass or size. 243

Cardiovascular system
The cardiac output is approximately 30% lower in GF rats compared to conventional controls, accompanied by a mild phenomenon of hemoconcentration which result in reduced blood supply to peripheral organs. 247,248Under normal oxygen conditions, the transcriptomic changes in the hearts of GF mice revealed 117 differentially expressed genes, with 73 genes upregulated and 44 genes downregulated. 249These changes implicate key biological processes such as cardiac function, cell proliferation, transcriptional regulation, and immune response. 249or instance, the upregulation of Amd1 may foster cell proliferation, while the downregulation of Cacna1d could affect the electrophysiological properties of the heart. 249These alterations might have short-term beneficial impacts on cardiac health but could also pose long-term risks for disease development.In contrast, under conditions of intermittent hypoxia and hypercapnia (IHH), which simulate obstructive sleep apnea syndrome, CONV-R mice exhibited 192 changes in gene expression, predominantly related to cardiac cell death and cardiac hypertrophy. 249Genes such as Bcl2l1, Cryab, and Gsn showed regulatory changes that could influence the heart's response to stress. 249hereas, GF mice displayed 161 gene expression changes, more closely associated with regulators of cardiac hypertrophy, including the downregulation of genes like Ace, Ankrd1, and Aplnr, and the upregulation of genes such as Cdkn1a, Fhl2, Rgs2, and Stat3. 249uring fasting, GF mice showed a significant decrease in heart weight, linked to a notable alteration in the pathways of cardiac metabolism. 250With the lack of microbiota, there is a reduction in the generation of hepatic ketone bodies, causing the hearts of GF mice to shift their dependence towards glucose as the principal energy substrate to maintain performance. 250The absence of the microbiota also adversely impacts vascular integrity, with these impacts being sexually dimorphic. 247Regardless of sex, GF mice exhibit reduced vascular contractility; however, male mice display increased vascular stiffness and inward hypertrophic remodeling, indicative of chronic blood flow reduction, while female mice exhibit outward hypertrophic remodeling, potentially associated with vascular aging. 247spiratory system GF mice displayed a 24% reduction in both nasal paranasal sinus mucosa and epithelial layer thickness, coupled with a 45% increase in collagen content and a 50% decrease in goblet cell count. 251Additionally, the nasal-associated lymphoid tissue (NALT) area in GF mice was reduced by 30%, indicating a compromised local immune response. 251Their lungs are characterized by a reduced number of alveoli, an enlargement in alveolar dimensions, and a decrease in mucus secretion. 252,253In room air, GF and CONV-R mice exhibit similar lung development and function, along with comparable pulmonary vascularization in both normoxia and hyperoxia; however, GF mice demonstrate reduced hyperoxia-induced lung injury and improved lung function compared to CONV-R mice. 254This is because under hyperoxia, the pulmonary microbiota shifts favoring oxygenresistant species such as S. aureus, with this alteration preceding and correlating with the severity of lung inflammation. 255gestive system In terms of intestinal morphology, GF mice exhibit a reduction in both the total mass of the intestine and the overall surface area of the small intestine. 256The villi of the small intestine are slender and uniform, with shorter villi in the ileum and longer villi in the duodenum. 257The rate of cell renewal in the crypts of the small intestine is slower. 258,259A prominent feature of GF rats is the enlargement of their cecum, a condition that results from the accumulation of mucopolysaccharides, digestive enzymes, and water within the intestinal lumen. 260During periods of fasting, the cecum of GF rats expands considerably, and the majority of the proteins and carbohydrates within its contents originate from within the body, indicating that the small intestine's ability to effectively break down and assimilate these materials is compromised. 261Regarding intestinal motility, the intrinsic primary afferent neurons (IPANs) in the enteric nervous system of GF mice demonstrate reduced baseline excitability, as indicated by an enhanced slow afterhyperpolarization (sAHP), leading to an extended refractory period following the initial neuronal firing. 262,263This disruption potentially affects the rhythmicity and coordination of gut movements, resulting in irregularities such as abnormal transit rates-either slowed or accelerated-and irregular peristalsis. 262Furthermore, GF mice showed a diminished response to the IKCa channel blocker TRAM-34, a drug that typically modulates gut motility. 262Their increase in muscular tissue in the cecum, characterized by elongated and hypertrophied muscle cells, which also leads to an extended transit time through the intestines. 264Physiologically, there is a decrease in osmolarity within the small intestine, while the oxygen tension and electrical potential are elevated. 257Functionally, GF mice showed enhanced absorption of vitamins and minerals, with alterations in the uptake of other ingested substances. 265There is also a change in the enzymatic content of the feces, with increased levels of trypsin, chymotrypsin, and invertase. 266The feces of GF mice have a higher content of mucin (mucoproteins and mucopolysaccharides), and there is a reduction in fatty acids within the intestinal content, with a predominance of excreted unsaturated fats. 257While the inability to synthesize certain vitamins, GF mice/rats require additional dietary supplementation of vitamins like K and B. [267][268][269] However, these mice also experience an impact on fluid balance, evidenced by an increased intake of water. 265

Kidney function
The detrimental aspects of kidney health in GF mice are characterized by a significant increase in the expression levels of purine-metabolizing enzymes, such as xanthine dehydrogenase (XDH), which leads to higher urinary excretion of purine metabolites. 270Particularly, the production of 2,8-dihydroxyadenine (2,8-DHA), a nephrotoxic byproduct, is elevated, exacerbating adenine-induced kidney damage. 270Moreover, the fecal purine metabolite profile in GF mice is substantially altered, with higher levels of guanosine, inosine, xanthine, and urate, and lower levels of guanosine monophosphate (GMP), adenosine monophosphate (AMP), guanine, adenosine, adenine and hypoxanthine compared to mice with a normal microbiota. 270These alterations in purine metabolism and the presence of toxic metabolites contribute to the increased vulnerability of GF mice to kidney injury.

Internal metabolism
The thyroid gland of GF mice, which is responsible for iodine uptake and storage, showed a reduced ability to concentrate inorganic iodine and a decrease in basal metabolic rate. 271During the light phase, when resting and fasting, GF mice have a lower respiratory exchange ratio, signifying a reliance on fat oxidation for energy. 272Low liver glycogen levels at the end of the light phase may suggest a more rapid depletion of hepatic glycogen in these mice. 272Conversely, during the dark phase, when they are active and consuming food, their metabolism favors glucose as the main energy source. 272The liver's circadian gene expression is significantly altered, with a notable reduction in sex-based differences, which correlates with shifts in sex hormone levels and growth hormone secretion patterns. 273The diminished levels of ghrelin in these mice are rectified by exogenous administration, which normalizes gene expression and metabolism, underscoring the microbiota's role in hormonal and metabolic regulation. 273dditionally, GF mice showed impaired liver regeneration and diminished conversion of cholesterol and bile acids, suggesting a reduced capacity for metabolizing these lipids into necessary compounds or excretory products. 274The microbiota's influence on liver regeneration may primarily mediated through the regulation of bile acid and short-chain fatty acid metabolism, the activation of immune cells and cytokines including IL-6 and TNF-α, and the modulation of immune responses via metabolic byproducts such as LPS. 275mune system GF mice have a range of immune defects such as reduced in size and cellular content of thymus, an important immune organ, decreased circulating immune cell numbers (T cells, B cells and white blood cells) and antibodies. 243,276,277These animals showed significant underdevelopment of the gut-associated lymphoid tissue (GALT), including reduced volume and cellularity of the Payer's patches and mesenteric lymph nodes. 278Additionally, they have a decreased number of CD8+ T cells within the intestinal epithelial lymphocytes (IELs), 279 and a proportional decrease in CD4+ T cells, with notable differences in the quantity and distribution of Th17 cells. 280At the molecular level, there is a decrease in the expression of antimicrobial peptides in Paneth cells, 281 a reduction in secretory IgA produced by B cells, 282 and lowered expression of MHC II molecules and TLR 9 in intestinal epithelial cells, along with a decrease in IL-25 levels, which may affect microbial recognition and immune response. 283,284GF mice also have a reduced resistance to various pathogens, demonstrating decreased immune resistance and increased mortality upon infection. 285Moreover, immune abnormalities may also lead to Sjögren-Like Lacrimal Keratoconjunctivitis. 286 Neurological and behavioral alterations GF mice display higher blood-brain barrier (BBB) permeability from embryonic day E16.5 through E18.5, a condition that persists into adulthood. 287In these mice, the expression of key tight junction proteins, occludin and claudin-5, is lower, leading to a weakened BBB that allows more substances to enter the brain from the bloodstream which can affect brain development. 287hroughout their development, GF mice demonstrate pronounced differences in brain structure, maturation and behavioral performance. 288Compared with GF mice, CONV-R mice showed greater development in gray and white matter volume, fractional anisotropy and myelination, leading to enhanced spatial learning and memory, along with reduced anxiety and improved social novelty recognition. 288Notable disparities in the brain architecture of GF mice were observed, particularly impacting the amygdala and hippocampus. 289The amygdala showed a pronounced enlargement, with both aspiny interneurons and pyramidal neurons exhibiting dendritic hypertrophy. 289These neurons were characterized by an elevated count of dendritic spines, featuring an array of slender, stubby, and mushroomshaped profiles. 289In stark contrast, the ventral hippocampus of GF mice presented with pyramidal neurons that were not only shorter but also displayed reduced branching, alongside a diminished presence of stubby and mushroom spines. 289Moreover, while the dentate granule cells in GF mice exhibited a decreased complexity in branching, the overall spine density was found to be consistent with that of conventionally colonized counterparts. 289These extensive modifications may potentially contributing to the observed stress responsivity, anxiety-like behaviors and deficits in social cognition in GF mice. 290Although GF mice showed reduced social activity and elevated cortisol levels after social interactions, colonization with Fecalibacterium improves social deficits and normalizes cortisol levels after social interaction. 291From the notable reductions in nerve fiber diameter and an increase in hypermyelination, peripheral nerves and dorsal root ganglia demonstrated a significant delay in the development leading to skeletal muscle atrophy and impaired development as well as maturation of neuromuscular junctions, highlighting the crucial role of the microbiota in the proper growth and functionality of the somatic peripheral nervous system. 292In particular, the axons of intestinal wall nerves undergo significant degeneration with advancing age. 293Transplanting microbiota from CONV-R into GF mice alters the neural anatomy of the enteric nervous system and improves intestinal transit, facilitated by microbiota-regulated 5-HT release. 294The establishment of the mucosal glial cell network is a postnatal process, where they form a population that is continuously renewed and essential for the preservation of gut homeostasis. 295The gut microbiota plays a pivotal role in not only guiding the development of this network but also in the ongoing regulation and sustenance of these mucosal cells. 295productive system Typically, GF mice showed irregular estrous cycles, particularly due to the prolongation of the luteal or metestrus phases, which leads to a reduced frequency of the entire cycle. 296This irregularity may be associated with fluctuations in the levels of sex hormones.Moreover, GF mice generally have a lower reproductive capacity, which may manifest as lower mating rates, implantation rates, and litter sizes. 296Male mice showed delayed lumen formation in the seminiferous tubules and increased Blood-Testis Barrier (BTB) permeability at postnatal day 16, which correlated with reduced expression of intercellular adhesion molecules such as occludin, ZO-2 and E-cadherin. 297Additionally, male mice had lower serum levels of gonadotropins (LH and FSH) compared to CONV-R mice, and their testicular testosterone levels were also lower than those peers. 297In terms of sperm vitality, male mice may have lower sperm motility compared to CONV-R mice, potentially impacting fertilization ability and reproductive success. 296Notably, when GF mice are accidentally exposed to certain bacteria, such as B. distasonis and C. perfringens, their reproductive capacity significantly improves which is evidenced by the normalization of estrous cycles, increased mating and implantation rates, and enhanced sperm motility. 296Exposure to C. butyricum, capable of producing high levels of butyrate, restored the integrity of the BTB and normalized the levels of cell adhesion proteins in GF male mice. 297eletal system GF mice showed increased bone mass and altered bone matrix properties, characterized by reduced bone resorption, enhanced trabecular microarchitecture, elevated tissue strength, and increased bone mineral density, along with decreased wholebone strength compared to CONV-R mice. 298The elevated bone mass evident in increased bone mineral density and cortical thickness, is primarily due to reduced activation of the NOD1 and NOD2 signaling pathways. 299The reduction leads to decreased expression of inflammatory cytokines like TNFα and the osteoclastogenic factor RANKL, resulting in fewer osteoclasts and consequently less bone resorption. 299Additionally, the collagen structure of the bones in GF mice is altered, yet they do not exhibit reduced fracture toughness. 298These changes are accompanied by sexual dimorphisms, particularly in bone tissue metabolism, with male GF mice showing an enhanced signature of amino acid metabolism, while female GF mice display an increased signature of lipid metabolism. 298Male rats born germfree exhibit a significant acceleration in bone growth and changes in bone marrow cellular content following the reconstitution of the gut microbiota.Specifically, after the introduction of gut microbiota, these GF rats rapidly increased the bone mass of both cortical and trabecular bones, enhanced the bone tissue mineral density and improved the proliferation and hypertrophy of growth plate chondrocytes, leading to an increase in tibial length. 300In addition, there was an increase in the number of small-sized adipocytes and a decrease in the number of megakaryocytes in the bone marrow, indicating that the microbiota not only affects bone mass but may also regulate the bone marrow environment. 300The increase in short-chain fatty acids, particularly butyrate, may boost liver production of IGF-1, thus promoting bone growth through increased circulating IGF-1 levels. 300sculature Various types of skeletal muscles in GF mice, including the tibialis anterior (TA), gastrocnemius, soleus, extensor digitorum longus (EDL) and quadriceps, exhibited significant abnormal phenotypes. 301Overall, these phenotypes encompassed reduced muscle mass, muscle fiber atrophy, mitochondrial dysfunction, and impaired neuromuscular junction (NMJ) function. 301Specifically, muscle atrophy was associated with upregulated expression of muscle growth inhibitory genes Atrogin-1 and Murf-1, while the decrease in muscle quality and strength correlated with downregulated expression of IGF-1. 301lso, depletion of the microbiota results in elevated levels of the FXR antagonist TbMCA, which suppresses the FXR-FGF15 pathway and lowers FGF15, finally reduces ERK signaling necessary for muscle protein synthesis. 302The expression of musclespecific transcription factors MyoD and Myogenin was diminished, affecting the differentiation and regenerative capacity of muscle cells. 301Mitochondrial dysfunction was reflected in the reduced mitochondrial DNA content and SDH activity, linked to decreased expression of mitochondrial biogenesis-related genes such as Pgc1α and Tfam. 301NMJ impairment was related to reduced expression of Rapsyn and Lrp4, alongside lowered serum choline levels, affecting the synthesis and neurotransmission of acetylcholine. 301Additionally, amino acid metabolism changes in the muscles of GF mice were observed, with increased levels of glycine and alanine, potentially connected to increased expression of the Alt gene. 301Decreased expression of glycolytic genes like Pfk, Pk, Ldh and Pdh impacted energy production. 301Increased glycogen accumulation in the quadriceps may indicate impaired glycogen metabolism. 301These integrated genetic and metabolic changes led to poor performance in muscle strength tests for GF mice. 301Interestingly, transplanting the gut microbiota from pigs into GF mice replicated the muscle phenotype of the donor pigs, including higher body fat mass, a greater proportion of slow-contracting fibers, reduced fiber size, lower percentage of fast IIb fibers and enhanced fat production in the gastrocnemius muscle. 303ipose tissues GF mice have a lower percentage of body fat, despite the increased food intake 304 and the elimination of sex-based differences in adiposity. 305They also show a reduction in adipocyte size marked by an increased quantity of smaller adipocytes coupled with a diminished presence of larger ones. 306e inguinal subcutaneous adipose tissue (ingSAT) and perigonadal visceral adipose tissue (pgVAT) regions exhibit browning features. 306Within the white adipose tissue, there is an observable infiltration of eosinophils and M2-type macrophages, which are implicated in the browning process of the adipose tissue. 306A reduction in lactate levels alongside an elevation in (D)-3hydroxybutyrate levels within their brown adipose tissue (BAT) suggests an upregulated fatty acid oxidation pathway. 305It is known that they show resistance to diet-induced obesity through following mechanisms: increased levels of the fasting-induced adipose factor (Fiaf), which activates peroxisome proliferatoractivated receptor gamma coactivator 1-alpha (Pgc-1α) to enhance fatty acid oxidation, and heightened AMPK activity, which is crucial for energy balance and metabolism. 307They may compensate for the impaired storage and utilization of glucose in skeletal muscle by increasing the lipolysis in adipose tissue and promoting the browning of adipose tissue, thereby meeting their energy demands. 308However, this compensatory mechanism might also limit their immediate fuel supply during exercise, leading to a decrease in exercise capacity. 308In addition, the levels of very-low-density lipoprotein (VLDL) are decreased while highdensity lipoprotein (HDL) levels remain unaffected. 305in GF mice display reduced stratum corneum complexity, elevated transepidermal water loss and delayed healing post-injury, indicative of a compromised skin barrier. 309Decreased corneodesmosomes and downregulated genes crucial for keratinization and barrier integrity are observed. 309Notably, the aryl hydrocarbon receptor signaling pathway, key for skin homeostasis, shows reduced activity. 309Skin bacteria can enhance the production of inflammatory cytokine IL-1β, which in turn activates the IL-1 receptor and myeloid differentiation primary response 88 (MyD88) signaling pathway within keratinocytes. 310This activation is diminished in GF mice, which may partially explaining their reduced capacity for skin regeneration. 310ngevity and death Due to lack of potential infection by pathogens, GF mice have an extended average lifespan of 88.9 weeks, outliving CONV-R mice, which average 75.9 weeks. 311But under a restricted diet, equivalent to 80% of their usual intake, CONV-R mice significantly boost their lifespan to 117.5 weeks, while GF mice only increase to 109.6 weeks, showing that dietary restriction powerfully extends life, particularly in CONV-R mice. 311The deaths of GF mice are typically associated with gastrointestinal dysfunction, including intestinal atonia, an abnormally enlarged cecum (with the average weight of the cecum being approximately 15 times that of CONV-R mice at the time of death), intestinal volvulus, liver abnormalities, and degeneration of the kidneys. 312In contrast, the causes of death in conventional mice are more diverse, encompassing respiratory infections such as pneumonia, circulatory failure, intestinal volvulus, intestinal spasms, inflammations of the genital tract, peritonitis, and ear infections. 312ltogether, these findings demonstrate that the humans and other animals without microbiota are abnormal with severe deformities.Thus, to better characterize the functional dependence of animals on microbiota, the collective set of abnormal symptoms can be referred as "germ-free syndrome".5][316][317][318] In this context, germ free, or more precisely, the absence of core microbiota, assumes clinical significance as it signifies a shift in the paradigm of microbial influence on disease-from focusing on the presence of pathogenic microbes to contemplating the consequences of a lack of essential microbiome.However, caution should be exercised when extrapolating rodent germ-free syndrome to humans, as the degree of dependence on microbiota may vary. 319 ADAPT OR NOT TO ADAPT, THAT IS A QUESTION The relationship between the host and microbes has been a longstanding topic of interest among biologists.Examples that best illustrates their close relationship are that mitochondria and chloroplasts are cellular organelles that evolved through endosymbiosis, 320 with each playing a key role in cellular energy metabolism and photosynthesis, respectively.321,322 Mitochondria, which are thought to have originated from an ancient Alphaproteobacteria, emerged around 1.5 to 2 billion years ago.323 Chloroplasts, on the other hand, originated from cyanobacteria and are estimated to have been incorporated into their host cells around 1 billion years ago.324 Recently, the nitrogen-fixing cyanobacterium UCYN-A has been proposed as an organelle called the nitroplast in Braarudosphaera bigelowii, attracting significant interest.325 In addition to endosymbionts, 326 looking back through history, the term 'symbiosis' was first coined by Adolf Meyer-Abich in 1943 to describe the state in which more complex organisms live in association with simpler ones.327 In 1991, Lynn Margulis introduced the term 'holobiont' to describe a single organism and the collection of all the microorganisms within it, which highlighted symbiosis as a source of evolutionary innovation.328 However, "superorganism" 45,46 and "meta-organism" [329][330][331][332][333][334][335] have risen to prominence in contemporary literature and media, reflecting an extension with their original definitions. To e specific, introduced by William Morton Wheeler in 1911, 'superorganism' was primarily used to describe social insect colonies such as ants, bees, and termites, which exhibit a high degree of organization and integration.Within these colonies, individual members have clear divisions of labor and work collaboratively towards the survival and reproduction of the group, functioning as if the entire colony were a single organism.336 While Graham Bell in 1998 posits "metaorganism" as a singular multicellular organism like Volvox, serving as a good model for the study of the origins of multicellularity.46 After that, at the genetic level, the concept of 'hologenome', the combination of host genome and microbiome, was subsequently introduced by Richard Jefferson in 2007, emphasizing microbes as an essential component of organismal function. 337 Rosnberg and Zilber-Rosenberg further developed the theory of hologenome evolution in 2007/2008, stating that the holobiont and hologenome are independent units of evolutionary selection.[338][339][340][341] To resolve possible controversies, Bordenstein and Theis proposed ten principles to better understanding the hologenome and holobionts.44 Overall, they did not regard the organism as an independent organism but emphasizes holobiont and hologenome is the fundamental biological and evolutionary unit and all animals and plants exist as holobionts, these entities exhibit unique anatomical, metabolic, and immunological traits that contribute to their development and evolutionary processes.340 Their genetic information can transmissible across generations, collectively shaping the distinctive characteristics of the holobiont.340 Genetic variation within the hologenome stems not only from the host genome but also from the microbiome .340 The latter, with its capacity to adapt more swiftly to environmental changes, plays an essential role in the adaptability and evolution of the holobiont.340 For example, coral, a small and simple marine invertebrate contribute to the formation of coral reefs through their collective calcium carbonate secretions, not only possesses its own genome but also forms a holobiont genome with various microorganisms, such as Symbiodinium. 338he corals provide essential shelter and inorganic nutrients to Symbiodinium, while Symbiodinium supplies the corals with energy-rich organic matter through photosynthesis, meeting up to 95% of the corals' energy needs.342 These microscopic algae have undergone a series of adaptive evolutions in the process of adapting to their symbiosis with corals including photosynthesis, ion transport, synthesis and modification of amino acids and glycoproteins, as well as responses to environmental stress.342 The holobiont genome enables corals to rapidly adapt to environmental changes more swiftly than it could rely solely on its own genetic mutations.[343][344][345] In the melon and grape plants subjected to grafting experiments, a detailed analysis of the composition of the root endospheric microbial communities revealed a distinct pattern of deterministic assembly. 346To be more specific, the rootstock played a predominant role in recruiting the microbial community which means that the composition of microbial communities was influenced in a non-random manner by the genetic characteristics of the host plants.346 Vampire bat, one of the only three species of obligate blood-feeding mammals, whose genomes and microbiomes have co-evolved to meet the unique challenges posed by a hematophagous diet.347 The bats' genomes show adaptive changes for this lifestyle, including morphological adaptations such as sharp incisors and canines, sensory adaptations with the positive selection of the PRKD1 gene for locating blood vessels, digestive adaptations like the loss of sweet taste receptor genes and a significant reduction in the number of bitter taste receptor genes, and their immune systems have evolved to combat common blood-borne pathogens.348 Their microbiome have also undergone positive selection for genes that collaborate with energy production (involved in metabolic pathways such as the reverse Krebs cycle, enabling the derivation of energy from blood components), carbohydrate metabolism (enabling the breakdown and utilization of scarce carbohydrates found in blood), vitamin synthesis (including genes for biosynthesis of essential vitamins, such as carotenoids, which aid in immune function), fat storage (with key genes like glycerol kinase critical for the formation of triacylglycerol and fat storage, managing energy reserves), immune protection (enriched with protective bacteria like Amycolatopsis mediterranei, known for producing antiviral compounds, and genes from bacteria such as Borrelia and Bartonella, adapted for transmission by sanguivorous species), and metabolism of iron and urea (including genes for iron storage like ferritin light and heavy chains, and microbial genes like urease subunit alpha for urea degradation, addressing the challenges of high protein intake and nitrogen waste management).348 As a classic example of homogenome vertical inheritance, Buchnera aphidicola is an obligate intracellular symbiotic bacterium that forms a specialized mutualistic relationship with aphids, characterized by a streamlined genome that retains only the essential genes required for synthesizing amino acids vital to its aphid host, while lacking genes for cell surface components and cellular defense mechanisms, indicative of its adaptation to the stable environment within the host's bacteriocytes.349,350 This symbiotic bacterium reproduces within the aphid's specialized cells and is maternally transmitted to offspring, ensuring the continuation of the symbiotic relationship across generations. 351he interdependence between Buchnera and the aphid is manifested at the genomic level, with neither being capable of independent survival without the other. 352Currently, the evidence supporting the coevolution of hominids and microbes is gaining strength.Tracing the evolutionary threads of key gut bacteria such as Bacteroidaceae and Bifidobacteriaceae, revealing that these lineages have cospeciated with humans, chimpanzees, bonobos, and gorillas over an extensive period spanning 15 million years.54 This profound coevolutionary synchrony has led to a harmonized diversification across the nuclear, mitochondrial, and gut bacterial genomes, indicating they have a deep-seated and intimate relationship.Research by Suzuki et al. further supports this, showing codiversification between human populations and their gut microbiota across Europe, Asia, and Africa.53 It highlights the emergence of microbial strains with population specificity, potentially due to a shared evolutionary history, and species that have adapted to host dependency with traits like reduced genomes and sensitivities to oxygen and temperature.53 Moreover, the earliest fossil records indicate that the origins of enterococci can be traced back to the time of animal terrestrialization, approximately 425 to 500 million years ago.353 The diversification of enterococci has paralleled that of their hosts, particularly following the rapid emergence of new species after the Permian-Triassic extinction event. 353Despite constituting less than 0.1% of the human gut microbiome, enterococci have become prominent multidrug-resistant, hospital-adapted pathogens.353 This adaptability is largely attributed to the hardened cell wall they developed during the early terrestrialization process, along with their resistance to desiccation, starvation, and disinfectants, traits that have been crucial for their persistence in the modern hospital environment.353 Undoubtedly, the concept of "holobiont" and the "hologenome theory" offer profound insights into the understanding of the aforementioned phenomena.Although these concepts redefine the composition of individual unit, they do not fundamentally rewrite the theory of natural selection proposed by Charles Darwin and Alfred Russel Wallace.44,354 That is, natural selection remains the primary mechanism driving evolutionary change, the inheritance and variation of advantageous traits in the struggle for existence, leading to the gradual adaptation of species and the emergence of new ones.44,354 However, holobiont and hologenome extend the classical theories by incorporating the genetic contributions of the microbiome into the considerations of biological evolution and adaptive change, thereby offering a supplement for the modern evolutionary synthesis.355 As a simple understanding, natural selection can operates at multiple levels, including genes, individuals, populations, species, ecological communities, and holobiont entities, collectively shaping the diversity and evolution of life.356 In our limited comprehension, the concepts of holobiont and hologenome currently have areas that require refinement especially when apply these concepts to humans.Firstly, when considering the life cycle, these theories struggle to adequately explain the sequence of appearance between the host genome and the microbiome.For humans, the normal embryonic development occurs in the absence of live microbes within their own body-previous discussions have touched upon the fact that if there is an impact, it is more likely due to contamination.Microbes colonize during and after birth, and the assertion that all organisms are holobiont and homogenome may lead to the paradox that unborn baby are not considered biological entities. Fro a genetic perspective, the inheritance of microbes is not high-fidelity.Vertical transmission (through the birth canal of the mother) or horizontal transmission (acquired from the surrounding environment) are essentially forms of contact transmission, which cannot even be considered inheritance, accompanied by a certain degree of randomness. The eample of Buchnera aphidicola is one of the exceptions that can be explained by the existence of hologenome inheritance, but it does not imply that other modes do not exist. The divrsity of life constantly reminds us that when interpreting biological phenomena, we should allow for the existence of multiple patterns.Although we prefer to use a single pattern to explain all phenomena, this may limit our further thinking.When considering the driving phenomena behind the co-evolution of multicellular organisms with their microbes, it appears that the underlying potential causes have not been well pointed out, and currently, more attention is given to a general phenomenon.More research is needed to verify whether the evolution of microbes is towards a direction more beneficial to the host or towards a direction more beneficial to the microbes themselves.Determining who leads whom is crucial.We may consider that the host's proactivity is the most likely driving force behind the happening of homogenome, a notion that is also evident from the discussed examples, just as the ecological environment of the Earth largely dominates the diversity of life, and the host can also be the natural selective force for microbes.In terms of application, the hologenome theory may not be a host-centered theory.Therefore, there is a lack of refinement in the framework of their interrelationship with the host's interests at the core.
To better delineate the evolutionary boundaries between the human genome and the microbiome, we can distinguish their characteristics using the terms "innate genome" and "adaptive genome."The innate genome, humans are born with, forms the foundation of our biological identity, comprises a complete set of human nucleic acid sequences that can be inherited across generations following "Mendelian inheritance" and develops into organ systems, performing physiological functions in an organized manner.Conversely, the microbiome is acquired, regulated, and subject to dynamic changes, resulting in extensive biological crosstalk with the innate genome, ultimately affecting health and disease development (Fig. 3).8][359] However, the notion of the microbiome as a "second genome" to humans maybe inappropriate. 360The terms "first" and "second" imply a sequential relationship within the same entity, whereas humans and their associated microbes are distinct species with their own evolutionary trajectories.The innate and adaptive genomes, together with the concepts of histological, immunological, host and homeostatic regulation proposed in this paper form a systematic framework to help us better understand the human-microbiome relationship and its interactions at all levels.Next we further discuss how the microbiome acts as an adaptive genome.
Adaptation to the selection, control and regulation of the host Immunological and neurological regulation.The immune system plays a crucial role in regulating the microbial community by utilizing both innate and adaptive immunity, and mucosal and systemic immunity.The central nervous system and the peripheral nervous system are indispensable components in the coordination of immunity.The brain engages in intimate communication with the immune system through its extensive neural networks and chemical messengers.Specifically, neurons in the central amygdala and the paraventricular nucleus of the hypothalamus express corticotropin-releasing hormone (CRH). 361The axons of these CRH neurons extend to the spinal cord and sympathetic nervous system, ultimately connecting with the splenic nerve to interact with immune cells in the spleen. 361Within the spleen, norepinephrine stimulates T cells to produce acetylcholine, a neurotransmitter that further acts on B cells, particularly through the α9 subtype of nicotinic acetylcholine receptors (nAChRs), promoting their activation and differentiation into plasma B cells. 361hese plasma B cells are responsible for antibody production in circulation, a crucial component of the adaptive immune response. 362Indeed, the nervous system also can detects inflammatory cytokines like IL-1β, TNF-α, and IL-6 via sensory nerve terminals, relaying signals through the vagus nerve to the nucleus tractus solitarius in the brainstem initiating a neuroimmune feedback loop that regulates body inflammatory responses. 363he recognition and regulation of commensal microbes are carried out by CD4+ effector T cells and innate lymphocytes. 364T cell receptors (TCR) recognize widely conserved, highly expressed bacterial surface antigens. 364Th17 is induced by commensal microbes to express cytokines IL-17 and IL-22, which maintain a non-inflammatory state, while pathogenic bacteria induce Th17 cells to express IFN-γ and TNF, leading to an inflammatory state. 3650][371] However, when microbes invade the epithelium, they bind to FcαRI (CD89) on proinflammatory cells and cause a local inflammatory response. 372IgA also has the ability to modulate microbial gene transcription, promoting the growth of beneficial bacteria while inhibiting the growth of harmful microbes. 373A recent interesting study has found that in the aged pituitary, growth hormone-secreting cells can independently produce IgA without the need for B cells, a process that is positively regulated by the diversity of the gut microbiota. 374It is speculated that this might serve as a compensation for the aging immune system, although the low level of IgA signals in pituitary cells has limited further understanding of this issue. 374ntimicrobial peptides (AMPs) or host defense peptide (HDPs), possesses antimicrobial activity in response to infection 375,376 The secretion of IL-18 by enteric neurons is necessary for the expression of AMPs in goblet cells. 377Specifically deleting IL-18 in enteric neurons leads to a decline in the mice's resistance to Salmonella typhimurium infection, manifested by greater weight loss and increased bacterial abundance in the cecum, liver, and spleen. 377In fact, AMPs exert their effects with distinct specificity with not merely functionally overlapping. 375For instance, Paneth cells secrete Peptide YY, an antifungal peptide that is released into and retained within the intestinal mucus layer. 378This peptide selectively inhibits the invasive and pathogenic hyphae of Candida albicans while having minimal impact on the yeast form that coexists with the human body. 3780][381] Fruit fly mutant analysis has detailed the distinct roles of antimicrobial peptides DptA and DptB, with DptA combating the pathogen Providencia rettgeri and DptB targeting the Acetobacter. 382The presence of these genes in Dipteran insects is closely tied to the microbes in their environment, with gene loss or pseudogenization occurring in the absence of these specific microbes. 382nterestingly, human AMPs (e.g.LL-37, a member of the cathelicidin family) were found to synergize with the Sh-Lantibiotics, secreted by the skin commensal S. epidermidis and S. hominis, to efficiently and selectively kill the S. aureus. 383So decreased secretion of AMPs such as defensins, lectins, lysozyme, ribonucleases, and cecum toxins can leads to increased susceptibility to certain pathogens. 384,385Therefore, in this section, it may be more accurate to understand AMPs as microbial regulatory peptides (MRPs) as they do not remove all microorganisms, but rather play more of a regulatory role.
Host sources.Sources of oxygen, carbon, nitrogen, electron transport chain receptors, and trace metals from the host form a nutritional ecological niche that regulates the selection and abundance of microorganisms.The colonization of facultative anaerobic bacteria gradually transforms the aerobic environment of the early intestine into an anaerobic environment, which favors the survival of obligate anaerobic bacteria. 41Obligate anaerobic bacteria further increase the oxygen consumption of IECs by producing metabolic products such as SCFAs, inducing the expression of hypoxia-inducible factor 1 (HIF-1)-related genes, affecting the metabolism of IECs, enhancing the tight junctions of IECs and promoting the production of mucus and antimicrobial peptides, thus shaping the microbiota group. 41,386,387In pigs, Yang et al. indicated that a 2.3 kb deletion in the ABO blood group gene, which occurred millions of years ago, led to a decrease in the concentration of N-acetylglucosamine (GalNAc) carbon sources in the intestine, directly affecting the nutritional metabolism of the family Erysipelotrichaceae and reducing its abundance. 388In contrast, in humans, it is Faecalibacterium prausnitzii and Collinsella aerofaciens that are capable of utilizing GalNAc. 389Bacteroides acidifaciens and Akkermansia muciniphila can utilize host-derived mucin as the nitrogen source. 390The latter is considered a potentially beneficial probiotic that can effectively regulate the host immunity and metabolism. 391It is worth noting that electron transport chain receptors from the host also flexibly regulate the microbiota.The epithelial cell NADPH oxidase 1 (Nox1) produces hydrogen peroxide (H2O2), preventing anaerobic Fig. 3 The meaning of adaptive genome.Human sperm and egg form the innate human genome.Microbes, through various selections, become the adaptive genome.Adaptive genomes may adapt to host selection and regulation, the dynamics of established microbial communities (which may promote, inhibit or remain neutral), [698][699][700] exposure to different diets and drugs, and fluctuations in the external environment.DASH: Dietary Approaches to Stop Hypertension bacteria from surviving in the inner layer of the mucus and crypts. 392Trace metals play critical roles as structural and cofactor elements in approximately one-third of proteins; however, excessive accumulation can lead to metal toxicity. 393Essentially, the body can suppress microbial replication, transcription, metabolism and survival by limiting or sequestering metals (such as iron, zinc, manganese, and copper) in the mucosal barrier and circulation. 393,394Immune cells can also employ a metal intoxication strategy by using zinc and copper to fight microbes in lysosomes. 393This "nutritional immunity" has recently been elegantly reviewed and may be exploited for the development of novel antimicrobial therapies. 393tracellular vesicles.Host-derived extracellular vesicles (EVs) are a type of vesicle secreted by cells into the extracellular space. 395he nucleic acids carried by EVs, including miRNAs, circRNAs, and IncRNAs, have been shown to regulate microbiota. 396iRNAs in EVs can enter bacteria and regulate microbial gene transcription.For instance, miR142a-3p secreted by IECs can bind to targets in the commensal bacterium Lactobacillus reuteri, promoting its growth. 397Secretion of factors like IL-11 in response to the microbiota can influence the expression of host cellular circRNAs, subsequently modulating the levels of corresponding miRNAs. 398Interestingly, this host response affects the capability of cancer cells to metastasize. 399Moreover, the IncRNA expression profiles of germ-free mice differed significantly from those of conventionally raised mice and can be used in distinguishing between colonized E. coli strains or fecal-derived microorganisms. 179rmones and metabolites.Hormones and metabolites circulating in the host body also affect the regulation of microbiota.Lyte and Ernst pioneered the field of microbial endocrinology, noting the impact of stress-activated neuroendocrine hormones on bacterial growth. 400Their work laid the foundation for subsequent discoveries that microbes possess hormone receptors, suggesting a role in intercellular messaging. 401Specifically, the gut microbiota of castrated male mice was more similar to that of female mice, suggesting that androgens may play a role in regulating the microbiota. 402Estrogen can reduce the abundance of Proteobacteria by activating estrogen receptor beta (ERβ) and increasing αdiversity of the gut microbiota. 403Ovariectomy (OVX) leads to increased levels of LPS in the serum, elevates the ratio of Firmicutes to Bacteroidetes. 404The decline in sex steroid levels, commonly experienced during menopause, enhances intestinal permeability and initiates inflammatory responses in the small intestine and bone marrow.This process stimulates the production of osteoclastogenic cytokines such as TNFα, RANKL and IL-17. 405Consequently, these cytokines promote osteoclast formation and activity, leading to bone loss, which may underlie the development of osteoporosis in postmenopausal women. 4057][408] Host metabolites, such as serum lactate, can be utilized by Veillonella atypica to produce propionate, which provides more energy to meet the body's metabolic demands during exercise. 409egnancy.During normal pregnancy, women experience significant changes in their hormonal, immune, and metabolic profiles, which are reminiscent of the characteristics of metabolic syndrome. 410Research has indicated that the gut microbiota of pregnant women undergoes substantial alterations throughout gestation, particularly in the third trimester, where there is a notable increase in microbial diversity and a rise in the relative abundance of certain bacterial groups such as Proteobacteria and Actinobacteria. 411These shifts in microbial composition are closely associated with the host's state.
From a macroscopic perspective, during human evolution, various modes have been developed to regulate the commensal relationship with the microbiome.Variations in regulatory patterns caused by host factors such as gender dimorphism, [412][413][414] age (developmental stage), 415 genetics (ethnic origins, genetic mutations), 416,417 behavior (sleep, stress, exercise), [418][419][420] and disease status (infection, activity, organ failure) 421,422 may affect the variability of adaptive genomic profiles among individuals.
Adaptation to variations in diet Food serves as a fundamental requirement for sustaining human growth, reproduction and health. 423][426] Differences in the gut microbiota across regions and countries may be attributed to dietary practices. 427Microorganisms can rapidly and reproducibly respond to ingested nutrients, exhibiting a simultaneous and consistent convergence in the changes observed between humans and other mammals. 334,428,429Studies have suggested that dietary protein (e.g.animal protein, whey protein isolate, and pea protein isolate) can enhance microbial diversity, whereas a high-fat diet (HFD) can significantly reduce the abundance of gut Lactobacilli and increase the proportion of Clostridium, Bacteroides and Desulfovibrio (producing propionate and acetate). 424The genus Desulfovibrio can also produce significant amount of leucine when exposed to HFD, which activates the mTORC1 signaling pathway in myeloid progenitors, fostering the differentiation and proliferation of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs). 430This mechanism is integral to the "gut-bone marrow-tumor" axis, facilitating the progression of cancers including breast cancer and melanoma. 431Digestible carbohydrates, such as starch and sugars (glucose, fructose, sucrose and lactose), can increase the abundance of Bifidobacterium and decrease the abundance of Prevotella, whereas, artificial sweeteners show the opposite trend. 424,432Polyphenols, found in various fruits, vegetables, seeds, and beverages (e.g., beer, wine, juice, coffee, tea, and chocolate), and in small amounts in grains and legumes, can significantly reduce the number of pathogenic bacteria, such as Staphylococcus aureus and Salmonella enterica, while enhancing the abundance of beneficial microorganisms. 424Of all the nutrients, the effect of dietary fiber on microbes has been the most widely and intensively studied due to their wide-ranging benefits for human immunity and metabolism. 433Dietary fibers may influence the gut microbiota by: (1) providing direct nutrient substrates, such as resistant starch, which is utilized by Ruminococcus bromii in the colon; 434 (2) activating microbial enzyme systems, such as Bifidobacterium, which uses its enzymatic capabilities to effectively metabolize galactooligosaccharides, thereby increasing its presence and activity in the intestinal tract; 435 (3) regulating environmental pH, where the production of butyrate from fiber fermentation lowers intestinal pH and inhibits the growth of non-adaptive bacterial species; 436 and (4) facilitating cross-feeding, where primary decomposers such as R. bromii breaks down resistant starch into short-chain fatty acids, which are subsequently utilized by secondary decomposers such as Faecalibacterium prausnitzii. 437A recent comprehensive assessment supports specific dietary fibers selectively enhance the abundance of certain gut bacteria-carrageenan increases Phascolarctobacterium, Prevotella, and Treponema; xylan boosts Butyricimonas; arabinogalactan augments Bacteroides; and β-glucan promotes Lactobacillus. 438Conversely, the abundance of Clostridium perfringens and Bacteroides fragilis is reduced by a range of fibers, including arabinoxylan, apple pectin, xylan, arabinogalactan, xanthan gum, guar gum, carrageenan, glucomannan, and β-glucan. 438In particular, Cynthia et al. reviewed over 1500 human fiber intervention studies, integrating 16 S rRNA amplicon data from 2368 gut microbiome samples from 488 participants. 439he above robust dataset offers strong clinical evidence, enabling a comprehensive assessment of human microbiome's response to various types of dietary fiber. 439The interplay between diet and the gut microbiome contributes to the fluctuation of serum metabolites, which in turn correlates with the alteration of specific clinical indices.For example, systolic blood pressure is specifically decreased by the consumption of vegetable oil, which enhances the abundance of the Blautia and concurrently lowers the serum levels of 1-palmitoyl-2-palmitoleoyl-GPC (16:0/16:1). 440In addition, fruit consumption exerts a similar blood-pressure-lowering effect by elevating the serum levels of threonate, a metabolite enhanced by Blautia. 440Overall, different dietary patterns, such as Western diet, 441 Mediterranean diet, [442][443][444][445] veganism, 446 Nordic diet, 447 Dietary Approaches to Stop Hypertension (DASH) diet, 448 Carnivore diet, 449 Ketogenic diet, 450 plant-based diet, 451 intermittent fasting, 452 and traditional Asian diets, 453 provide various combinations of nutrients, thereby changing the composition and richness as well as function of surviving microbes.Harnessing dietary interventions to modulate the microbiota represents a promising avenue for optimizing human metabolism. 426,454aptation to environmental conditions In contrast to genetics, environmental factors are better able to explain the variations observed between microbial communities. 455,4568][459] For instance, the hpEurope population demonstrates a higher degree of genetic variability as a consequence of multiple historical waves of human migration. 457,458Analysis of 13,000 publicly available metagenomic samples using artificial intelligence has revealed a close relationship between microbial genes and their habitat. 460ystematic summary has been reported indicating striking differences of the gut, oral cavity, respiratory tract, skin and urinary tract microbiome across different populations worldwide. 461Within 3224 Chinese individuals, researchers found that geographical factors are the most significant external influences on the composition of the gut microbiome, with the similarity of the microbiomes among individuals being inversely proportional to their geographic distance. 440Interestingly, gut microbes share approximately 48.6% similarity in the cohabitation scenario. 456urthermore, airway microbiome can serves as a mediator in the influence of environmental pollution factors on respiratory system health. 462With the transition of humans from a primitive hunting and farming lifestyle to an urban lifestyle, there has been a decline in microbiome diversity.Specifically, the gut microbiomes of primitive civilizations were characterized by high abundance of Prevotella, Aspergillus, Spirochetes and Clostridium, whereas those of urban dwellers typically contain Bacteroides, Bifidobacteria and Firmicutes. 461Western urban populations appear to have lost microorganisms such as dense intestinal spirochetes, possibly due to multiple factors, including changes in dietary habits and modern drug treatments, as this microorganism is still retained in other primates (excluding the effects of climate change). 461Of all the microbiomes, the skin, which is exposed to the natural environment, appears to be the most affected.For example, in rural areas, they were more exposed to soil and environmental microbial sources, while in urban areas, participants worked indoors and had less access to these sources. 463These environmental differences may explain the differences in the abundance of Trabulsiella and Propionibacterium in the participants' skin. 463A systematic review reported that greenspace exposure was associated with increased microbial diversity as well as alterations in the overall composition of the microbiota in the gut and skin. 464pecifically, there were increases in the relative abundance of beneficial bacteria (e.g., Ruminococcaceae) and decreases in the relative abundance of harmful bacteria (e.g., Streptococcus and Escherichia/Shigella). 464However, regionalized differences also pose challenges in establishing uniform microbial-related predictors and models. 465The space environment, which includes microgravity and radiation, could profoundly influence on the physiology, genetics and community composition of microorganisms.During short-term spaceflight, the skin microbiome exhibits a temporary increase in viral populations, including Uroviricota, Cressdnaviricota and Phoxiviricota. 466In the oral microbiome, there is an observed increase in bacterial groups associated with periodontal disease and dental caries, such as Fusobacteriota, with notable species like Fusobacterium hwasookii, Fusobacterium nucleatum and Leptotrichia hofstadii. 466Spaceflight also enriches microbial genes related to phage activity, toxin-antitoxin systems and stress responses across multiple body sites, indicating adaptive changes of microbes to the stressors of the space environment. 466Although most of these changes are transient, such as Corynebacterium species, showed a temporary decrease in transcriptional activity, 466 some bacterial groups in the skin microbiome, like Acinetobacter spp.demonstrated a persistent reduction. 466aptation to various medications Medication can alter the intestinal microenvironment, influencing microbial growth or undergoing direct microbial metabolism, ultimately modifying the composition and function of the microbiota. 467,468Antimicrobial resistance is a common survival mechanism in both pathogens and commensal bacteria. 469nitially, six-month antibiotic treatments for tuberculosis disrupt the gut microbiome, allowing drug-resistant pathogens to dominate. 470However, commensals soon overtake them through competitive adaptation. 470Additionally, non-antibiotics like antidepressants can increase mutation rates and speed up the horizontal transfer of resistance genes by activating bacterial defense mechanisms. 471With the expansion of research, our understanding of the effects of drugs on microorganisms has extended to more medications. 472Proton pump inhibitors (PPIs), a type of medication used to treat digestive disorders, can reduce the acidity of gastric fluid and increase the number of oral microorganisms that migrate to the intestine. 473,474Metformin, a traditional medication for lowering glucose, can increase the abundance of mucin-degrading bacteria Akkermansia muciniphila and butyrate-producing bacteria. 475In addition, data from 2173 individuals in the European Heart and Metabolic Disease cohort showed that 28 drugs significantly affected the microbial characteristics, demonstrating a combination, cumulative and dose-dependent effect. 476The synergistic effect of multiple drugs can redirect the host microbiota to a more favorable state, and an increase in the number of antibiotic courses is associated with an increase in the abundance of harmful microorganisms. 476Microorganisms can chemically modify oral medications to produce different functional and pharmacological properties.For example, 5-aminosalicylic acid (used to treat ulcerative colitis) relies on colonic bacteria to cleave azo bonds and release active drugs in the colon; 477 and digoxin (used to treat heart disease) can be inactivated by Eggerthella lenta. 478Similarly, Gardnerella vaginalis, the dominant bacterium in the vagina, can predict poor outcomes for tenofovir (a pre-exposure prophylactic drug for HIV infection), whereas Lactobacilli can increase its efficacy threefold. 479The β-glucuronidase of commensal bacteria can convert irinotecan (a prodrug for colon cancer treatment) into a toxic form, killing intestinal epithelial cells and causing severe diarrhea. 480In a study by Zimmermann et al. of the 271 oral medications tested, twothirds could be metabolized by various strains of intestinal bacteria, and each strain could metabolize 11-95 drugs. 481ecently, a team established a drug metabolism model based on the genomes of 7,302 microorganisms to explore personalized prediction and analysis. 482][485] Further studies of the interplay between the adaptive genome and the innate genome's drug response, absorption, distribution, metabolism, and excretion show potential in predicting disease treatment efficacy and improving individual drug efficacy levels, leading to Precision-Comprehensive Drug Microbiology.

Adaptation to established microbial communities
The human microbiota community is a complex ecological network.Established microbial communities influence newcomers positively, neutrally, or negatively. 486In vitro co-cultures of fecal microbiota show that 51.67% of these relationships are neutral. 487ommensalism, which make up 21.67% of interactions, occur when one organism benefits from another without harm, or both benefit from each other. 488This often occurs through crossfeeding between microbes, such as when Acetobacter pomorum obtains lactic acid from Lactobacillus plantarum and in turn produces amino acids essential for the growth of Lactobacillus plantarum. 489In addition, bacteria can cooperate to form biofilmsaggregations that enhance protection and competitive advantage by conferring antibiotic resistance to their members. 490Interestingly, a recent discovery involves an oral Saccharibacteria isolate (TM7x) that protects its host bacterium, Schaalia odontolytica (XH001), from predation by the lytic bacteriophage LC001. 491ntagonistic relationships account for 18.33%, where one organism inhibits another without harming itself. 492Some bacteria can secrete antibiotics or other inhibitory substances to suppress competitors and maintain resource dominance. 493Competitive interactions, which account for 5%, involve two species competing for the same resources and adversely affecting each other. 494For example, in vitro cultures of Intestinimonas butyriciproducens and Shigella flexneri showed inhibited growth when in close proximity. 487Exploitative relationships, which account for 3.33%, are similar to predatory relationships in which one organism uses another as a resource. 495A classic example is bacteriophages, which are often described as obligate predators of bacterial hosts, achieving reproduction through mechanisms such as generalized transduction, specialized transduction, and lateral transduction. 496owever, Shkoporov et al. suggested that at the population level, phage-bacteria interactions may facilitate long-term coexistence. 496In the face of constant phage threats, bacteria are forced to continuously produce genotypic and phenotypic variants, reducing the sensitive subpopulation through lysis and allowing the spread of resistant mutants, thus increasing intraspecies diversity. 496It is crucial to emphasize that higherorder interactions within microbial communities are key drivers explaining the characteristics of microbial consortia. 497Quantifying the genetic adaptability of E. coli in different communities (from two to four species) suggests that these higher-order interactions significantly affect microbial gene expression and function. 497Even in simple microbial communities, the dynamics of interactions are complex and essential for understanding microbial functional mechanisms.In fact, the specific microbes and the nature of their co-occurrence relationships can vary significantly between organs and are influenced by a range of factors including pH levels, immune responses and the presence of specific nutrients or other environmental conditions within each organ's microenvironment.For example, the oral cavity and the large intestine are characterized by a higher incidence of coexclusive relationships among microbes, while other organs show a more pronounced presence of co-occurrence relationships. 91nraveling adaptive mechanisms is crucial for predicting the regulation of community dynamics and enhancing the success and stability of microbial transplants.However, this endeavor presents significant challenges.In this context, the study of keystone taxa -first introduced by Paine as species that play a critical role in the stability of their ecosystems may be a good strategy. 498,499ST OR META HOST The introduction of the adaptive genome in above context can led to reconsideration of our understanding of the host, transitioning from a 'host' (innate genome) to a 'meta-host'.As a meta-host, it offers a unique ecological niche for other organisms, thereby affecting the host's susceptibility to infections, the pathogenicity of the infecting agents, and the severity of diseases (Fig. 4).500 Specifically, Miller et al. found that, compared to traditional mice, which are not typically suitable hosts for nematodes and tapeworms, were able to develop seemingly healthy and reproductive adults in germfree guinea pigs when infected with Nippostrongylus muffs, Fig. 4 Original host (conventional host model) and Meta-host (ecological host model).The meta-host is used to describe conventional host that exhibit marked differences in colonization, susceptibility and pathogenicity to microorganisms following microbial accession.This phenomenon is the result of the dynamic integration of the adaptive genome with the innate genome and corresponds to the human ecological perspective Nematospiroides dubius and Hymenolepis nana. 501The study also indicated that the destruction of commensal microorganisms led to increased susceptibility to Salmonella infection in mice treated with antibiotics (streptomycin) after infection with a lower titer. 196In contrast, Entamoeba histolytica is known to be pathogenic in the intestinal tract of traditional guinea pigs, but not in germ-free mice.When E. coli was added to the inoculum, intestinal damage occurred, which was not caused by E. coli alone. 502,503Patients with nontuberculous mycobacterial lung disease (NTM-LD) exhibit a significant perturbation in gut microbiota, particularly marked by a decrease in Prevotella copri, which is strongly correlated with both the occurrence and severity of NTM-LD. 504This is accompanied by a reduction in TLR2 activation activity and a discernible immunosuppressive effect within the lungs. 504ngela Wahl and colleagues developed a germ-free humanized mouse model that demonstrates the human microbiota significantly enhances the infection and pathogenicity of Epstein-Barr virus (EBV) and human immunodeficiency virus (HIV). 505The presence of a normal microbiota in conventional humanized mice (CV-BLT) promotes more frequent EBVinduced tumorigenesis and higher levels of HIV replication in the gut and systemic circulation. 505In young South African women, it has been discovered that the diversity of the cervicovaginal bacterial community is also closely associated with the risk of HIV infection. 506Specifically, communities with high diversity dominated by anaerobic bacteria other than Lactobacillus have been found to increase the risk of HIV infection by more than four times. 506Certain bacterial groups, such as Lactobacillus crispatus, are correlated with a reduced risk of infection, while others like Prevotella and Sneathia are associated with an increased risk by increasing the number of activated CD4 + T cells in the reproductive tract, which are the target cells for HIV infection. 506][509][510][511] These changes manifest as a striking enrichment of pathogenic microorganisms and a concomitant reduction in beneficial counterparts, and are closely associated with levels of biomarkers of inflammation and tissue damage suggesting a potential interplay between the microbial community and disease severity. 512The immune response and physiological milieu of infected individuals may induce these compositional changes, thereby compromising the host's antiviral capacity. 513,514The diminished biosynthesis of immunoregulatory metabolites, such as butyrate and L-isoleucine further impairs the body's ability to counteract viral invasion [515][516][517] and the increased infectivity of microbial agents exacerbates the clinical prognosis. 518While comprehensive investigations are warranted to unravel the complex effects of the microbial community on viral susceptibility and transmissibility, these findings necessitate a reevaluation of our defensive and therapeutic strategies in anticipation of future infectious diseases.Such efforts hold the promise of mitigating the disastrous consequences of rampant viral outbreaks on the world's population. 519Meta-Host model also show potential in the interpretation of organ transplantation heterogeneous outcomes.While the classic understanding points to genetic mismatches as the main cause of graft rejection, the unique microbiota of each individual might also play a crucial role.It can be evidenced by the extended survival of skin transplants in mice associated with the presence of Alistipes, suggesting that specific microbes could impact the host's physiological responses. 520Sequencing of 1370 fecal samples from 415 liver transplant recipients and 672 kidney transplant recipients also indicated that ecological shifts in the human microbiota are associated with increased mortality rates following transplantation. 521This underscores the potential therapeutic potential of targeted microbiota manipulation, such as with probiotics or microbiota transfers, to improve transplant success rates.

DO WE MANAGE A SLAVE TISSUE?
The captivating role microorganisms play in human physiology has sparked the prevalence of the 'organ' theory.In 1992, Bocci proposed that the gut microbiota is an overlooked organ that is critical for immune stimulation in humans. 522Subsequently, in 2006, O'Hara et al. further elaborated on this theory, calling for a deeper understanding of this hidden organ to unlock secrets related to human health as well as various infectious, inflammatory and tumor diseases. 523Since then, the gut microbiota has been popularized as an "organ" in academic and popular media.In 2013, Burcelin et al. pointed out that bacteria are also found in common tissues such as the liver and adipose tissue. 524The interaction between host tissues and microorganisms may provide new opportunities for disease diagnosis, immune regulation and nutritional applications, although their review did not consider it as an independent tissue rather named "tissue microbiota hypothesis". 524To further emphasize that host regulation is fundamental to the normal functioning of microbial organs, Byndloss and Bäumler proposed the "Germ-organ theory" in 2018 to describe how host dysregulation (such as epithelial dysfunction) can lead to the occurrence of non-infectious diseases (such as an increase in Proteus mirabilis). 525While the 'organ theory' deepens our appreciation for the significance of microorganisms, it has simultaneously sparked scientific debate.For example, Fucarino et al. contended against such perspectives, primarily because they adhered to the traditional definition of organs as structures composed of tissues with similar or varying embryonic origins within the human body, a criterion that microorganisms evidently do not meet. 526They proposed that the term "mucosal microbiota layer" of hollow organs more precisely encapsulates the role of microorganisms, as exemplified by the gut and respiratory tract ecosystems. 526However, this designation does not encompass the skin microbiota also falls short of offering a comprehensive systemic view on genetic and hereditary aspects.
In fact, the traditional definition can be appropriately adjusted based on the motivation behind the traditional terminology.Medical classification of cells, tissues (a group of cells), organs (a group of tissues), systems (multiple organs) and organisms (multiple systems) is helpful for scientists to focus on different levels of research.Owing to limited detection techniques, we initially did not have a clear understanding of the interaction of microorganisms in human physiology and pathology, and it is not surprising that we did not consider them as part of human tissues and organs.Overall, the 'organ theory' has stimulated greater research interest and clearly given microbial communities the attention it deserved.To better manage microbes in our bodies, several issues related to our understanding of body composition need to be addressed.Firstly, in our understanding, human microbiota are more like a component of the tissues that make up organs, rather than being stand-alone organs themselves.For example, in the gut, certain microbes play a critical role in the complete performance of digestive functions which can be consider as part of gut organ.The incomplete gastrointestinal function exhibited as we discussed in germ-free syndrome also corroborates this point.That is to say, a gut devoid of microorganisms cannot be considered a complete intestine and is unable to perform the full range of functions associated with a healthy gut.Similarly, the skin is an organ whose complete defensive function is facilitated by a covering layer of microbial tissue.Second, on specific classifications, the composition and functions of microbial communities vary greatly at different anatomical sites.Designating each distinct microbial community as a separate organ would unduly complicate the existing human organ classification system.Classifying microbial communities according to their specific anatomical locations is more consistent with traditional methods of tissue classification, such as the further categorization of epithelial tissues into overlying epithelium and glandular epithelium.Microbial tissues can be similarly categorized by corresponding anatomical locations, such as skin microbiota, gut microbiota, etc.Hence, regarding microbes as distinct organs isn't pragmatic.The final conundrum is that the traditional tissues are generally solid rather than fluid or dynamically mobile.Our previous discussions on how the microbiome adapts to and is regulated by host conditions provide a rationale for the emergence of the concept of "slave tissues".As a hypothesis, the multicellular organisms may exhibit a form of "slavery" towards microorganisms, maintaining a constant struggle that has driven long-term evolution.This concept, borrowed from sociology, can partially elucidate the variations in microbes across different developmental stages of an individual's life cycle.It also aids in explaining the acquired immunity and the models of host health and disease conversions.Most importantly, it expands the concept of histology to include an external, dynamic tissue, thereby resolving a nomenclature dilemma about microbiome in histology.Conversely, if microbes were to form an organimplying significant proliferation -they could have fatal consequences for the human body.Overall, these tissues have developed from adaptive genomes and possess physiological functions closely tied to the four master tissues (epithelial, connective, muscular, and nervous) (Fig. 5).Loss of control (microbial dysbiosis) of microbial tissue may lead to malignant cycles of cardiovascular, [527][528][529][530][531] respiratory, [532][533][534] digestive, 535 nervous, [536][537][538][539][540] endocrine and metabolism, [541][542][543] oral, 544,545 skin, 102,103,546 autoimmune, [547][548][549] urogenital, 550 mental disease, 551 and even cancers, [552][553][554] although the causality of related diseases so far is not always clear (Some of these diseases will be discussed in next sections).The formidable organizational structure of the human body's composition is profoundly systematic.This is precisely why, even when confronted with a great number of dispersed microorganisms resembling the human body, they still maintain a dominant position.Hence, it is prudent to regard microorganisms as a subservient or controlled component of the system.The "slave" perspective also makes hygiene practices (brushing teeth, washing face, bathing, disinfecting) more understandable and acceptable.Their development, the 'biofilm' and 'quorum sensing' abilities can damage our health. 555,556Therefore, we still need to control their location, limiting unrestricted growth and widespread communication, avoiding serious damage to other tissues (Fig. 5).
Attempts to classify microbial tissues with greater precision have ventured into new territory.The notion is that these so-called "slave tissues" can be systematically categorized through an ecological framework of classification.For example, in 2011, the MetaHIT team proposed the concept of 'enterotypes', dividing the gut microbiota into three types. 557They are robust classifications which are not influenced by nationality or region and characterized by a unique composition and metabolic signature of the microbial community: Enterotype 1, characterized by Bacteroides and efficient in fermenting carbohydrates and proteins; Enterotype 2, marked by Prevotella and its mucin-degrading capabilities, often in synergy with Desulfovibrio; and Enterotype 3, defined by Ruminococcus and Akkermansia, specializing in mucin binding and sugar transport. 557In subsequent research, the authors emphasize that enterotypes are not strictly separated categories but rather exhibit a tendency for clustering within a continuous spectrum of gut microbial community composition.They also provided a standardized procedure and guidelines for enterotype analysis to enhance the accuracy and comparability of research findings across studies. 558Different research teams, however, employing a variety of experimental approaches, algorithms, and analytical techniques, classified the gut microbiota into diverse categories. 559,560Recently, Senying Lai et al. conducted an extensive analysis of 3363 fungal sequencing samples from 16 cohorts across Europe, North America, and Asia, further delineating the four fungal enterotypes of the human gut (mycobiome). 561he Sacc_type enterotype, dominated by Saccharomyces cerevisiae, is more prevalent among younger individuals and correlates with a better intestinal barrier. 561In contrast, the Can_type enterotype, characterized by the abundance of Candida albicans, is enriched in the elderly and associated with an increased risk of various diseases and a compromised intestinal barrier. 561The Asp_type enterotype, led by Aspergillus species, shows a correlation with certain bacterial enterotypes, while the Asc_type enterotype is driven by either unclassified Ascomycota or Saccharomycetales. 561With advancements in capsule sampling and microbial visualization techniques, we may anticipate a shift towards more efficient classification that isn't solely reliant on fecal samples. 89,90,562In an analysis of the oral microbiome of 1500 Spanish adolescents revealed two predominant oral microbial community patterns, termed "stomatotypes". 563The first pattern is dominated by the genera Neisseria and Haemophilus, designated as the Neisseria-Haemophilus stomatotype (Stomatotype 1), while the second is characterized by the dominance of Prevotella and Veillonella, known as the Prevotella-Veillonella stomatotype (Stomatotype 2). 563They hypothesized that these stomatotypes may represent two potential optimal equilibria of the oral microbiome on a global scale, prevalent across various geographical regions, lifestyles, and age groups. 563Another example is vaginal Community State Types (CSTs), a classification system used to describe the composition of vaginal microbial communities in women of reproductive age. 110Specifically, CST I is characterized by the dominance of a single species of Lactobacillus, in particular L. crispatus. 564CST II is similarly characterized by Lactobacillus dominance, primarily L. gasseri. 116CST III is dominated by L. iners, although its association with vaginal health remains unclear. 116ST IV lacks Lactobacillus dominance and includes other facultative and obligate anaerobic bacteria such as Gardnerella, Prevotella, Atopobium, Sneathia, Megasphaera and Peptoniphilus. 116his microbial composition is associated with bacterial vaginosis (BV) and may increase the risk of several adverse health outcomes. 116Finally, CST V is dominated by L. jensenii. 110In summary, the detailed classifications of microbial types will empower researchers to discern various microbial community states, enhancing our comprehension of their relationship with human health.This advancement in turn will unlock significant clinical implications, including disease vulnerability, diagnostic accuracy, and the efficacy of medical interventions.

FROM HOMEOSTASIS TO HOMEOSTATIC REPROGRAMMING
In our previous discussions, we concluded the discourse on the hypothesis of the existence of foreign, salve-like tissues within the human body.Next, it is essential to re-examine the foundational theory of physiological medicine-homeostasis, as without homeostasis, there is no health.The internal environment, comprising extracellular fluids such as interstitial fluid, plasma, and lymphatic fluid, represents the environment in which the cell lives. 565In the 19 th century, French physiologist Claude Bernard introduced the concept of "interior milieu," emphasizing its stable and autonomous nature as a prerequisite for life.This property enables an organism to compensate for variations in the external environment. 565In 1929, the American physician Walter B. Cannon proposed the concept of "homeostasis", highlighting the dynamic stability and regulation of the internal environment. 566Currently, it is widely acknowledged that the internal environment maintains the dynamic stability of chemical composition (water, inorganic salts, and organic compounds) and physico-chemical properties (osmotic pressure, pH, temperature) in a coordinated manner across tissues, organs, and systems through neural, metabolic, and immune regulation. 567,568Maintenance of the internal environment's stability is critical for cellular metabolism and physiological functions of the body, and its disruption can result in diseases. 569The theoretical basis of the internal environment and homeostasis has made medical interventions possible.The hypotheses of adaptive genomes, slave tissue and germ-free syndrome, presents us with the opportunity to further expand the framework of homeostasis.Here, we introduce the concept of 'Homeostatic reprogramming' to describe a phenomenon in which the adaptive genome coordinates with the innate genome to deviate the scope and outcome of neuroendocrine and immune regulation from the original trajectory (Fig. 6a).In other words, the statement of maintaining homeostasis may not be accurate.A classic example of reprogramming is the Fig. 5 Slave tissue hypothesis.Microbial tissue is the additional fundamental tissue of the human body, a slave tissue alongside nervous, epithelial, connective and muscular tissues. 701,702The maternal microbiota exerts a regulatory influence on fetal growth and development and can partially transfer seed microbiota to the newborn through microbial exposure.Microbes that colonize in body site (including but not limited to the gastrointestinal tract, respiratory tract, reproductive tract, skin and urinary tract) play a vital role in digestion, immunity, neural regulation and metabolic crosstalk throughout human growth and ageing, and ultimately participate in the degradation of the body upon death. 37,415,703,704The human microbiota has undergone co-speciation, co-evolution, co-adaptation, and co-diversification with humans over a long period of time. 53Throughout the life cycle, factors such as mode of delivery, genetics, gender, diet, medication, environment and behavior (e.g.exercise) can potentially contribute to differential microbial tissue formation [705][706][707] possibility that 'healthy' body temperature is the result of a combined microbiota-host regulation.Intermittent changes in the external environment can induce changes in the resting metabolic rate, serum thyroid hormones and core body temperature in mice, while dynamic gut microbiota and their metabolites can provide the host with metabolic plasticity to regulate temperature fluctuations. 570Supporting this notion, antibiotic clearance of bacteria has been shown to damage Fig. 6 The conceptual model of homeostatic reprogramming mediated by commensal microbes.a The concept of 'Homeostatic reprogramming' is used to describe a phenomenon in which the adaptive genome (commensal microbiota) coordinates with the innate genome (human cell/tissues) to deviate the scope and regulation outcome from the original trajectory including body temperature, uric acid levels, glucose level, blood pressure, etc.The interplay between human life stages -from youth to old age -and microbial development -from increasing to decreasing diversity -overall results in different regulatory forces.b The conceptual model of cell-microbe co-ecology and cohomeostasis.Plasma, tissue fluid and lymphatic fluid form the internal environment of the human body's cell life.This internal environment is regulated by the neural, immune, and metabolic systems to maintain a dynamic homeostasis of physical and chemical properties such as temperature, pH, and osmotic pressure.The internal factors of cell differentiation, proliferation, ageing, damage, and apoptosis can affect this homeostasis.Human tissues are involved in shaping a physico-chemical and nutritional environment where external microorganisms can colonize, replicate, experience loss and die.On the one hand, human cells, and microorganisms in the digestive tract work together to metabolize nutrients from food.Microbes not only affect nutrient absorption, but also produce metabolites, vitamins, and potential "dark matter", which can enter the internal environment and affect its homeostasis.The imbalance of the internal environment also leads directly to the disruption of the microenvironment they form.The diversity, relative abundance, and products of beneficial, harmful, and neutral microorganisms (composition) are important indicators for assessing the environmental balance.On the other hand, microorganisms also participate in shaping the microenvironment by providing a barrier to respond to external environmental changes.This overall change regulates the susceptibility of the internal environment to external perturbations, acting another regulatory force for homeostasis body's thermogenic capacity. 570Recently, it has been shown that changes in the gut microbiota can predict the temperature course of hospitalized patients with sepsis, and that GF or antibiotic-treated mice have lower basal body temperatures than those harboring natural microbiota. 571When exposed to cold, animals can produce heat and maintain body temperature by activating brown adipose tissue (BAT) and browning of white adipose tissue (WAT). 572The absence of certain microbiota inhibits the increase in uncoupling protein 1 (UCP1) expression in BAT and reduces the degree of fat browning. 572These findings suggest that the presence of an adaptive genome may lead to reprogramming of body temperature, and that animals lacking microbiota may experience impaired thermoregulation.Of greater concern is that this may partly explain the curious phenomenon of a 1.6% average decrease in human body temperature since the 1860s, the use of antibiotics, improvements in hygiene and an increase in processed foods, accompanied by a decrease in microbiota diversity and abundance. 573,574Uric acid (UA), as another example, is the end product of purine metabolism in the human body, and excessive accumulation can lead to metabolic imbalances.Recent findings have revealed widespread purine degradation and anaerobic uric acid metabolism within the gut microbiota. 575,576This microbial process appears to compensate for the host's deficiency in UA-degrading enzymes, possibly stemming from a "thrifty gene" that gradually became inactive during human evolution to enhance adaptation to periods of hunger and cold by stimulating gluconeogenesis, increasing fat storage, and reducing fat oxidation. 577In rodent models lacking UA-degrading enzymes, depletion of gut bacteria results in severe hyperuricemia, while colonization with UA-consuming intestinal bacteria reduces UA levels. 575In retrospective patient studies, the use of antibiotics targeting anaerobic bacteria were associated with an increased risk of subsequent gout. 575Overall, the loss of UA-consuming microbes could partly account for the rising prevalence of hyperuricemia in modern times. 578Commensal microbes are also involved in the regulation of blood glucose homeostasis.Intestinal intrinsic enteric-associated neurons (iEANs), operating independently of central neural regulation, autonomously oversee functions such as intestinal motility and secretion. 579A subset of iEANs, characterized by CART+ neurons regulated by the gut microbiota, traverses from the intestines, establishing neural circuits with the liver and pancreas through the sympathetic nervous network. 579Activation of these neurons induces a decrease in insulin levels, a rise in blood glucose, and reduced food intake in mice. 579Microbial changes induced by non-nutritive sweeteners can causally lead to individualized alterations in blood glucose responses. 580GF mice exhibited lowered blood pressure levels, while population analyses of oral and gut microbial profiles indicated substantial correlations with blood pressure. 581The microbial regulation of blood pressure mechanisms has recently undergone comprehensive review. 582It is worth noting that changes in the microbiota that occur at each stage of development, from infancy to adolescence, adulthood, and old age, may show different perturbations.The presence of homeostatic reprogramming phenomena may require the correction of some relevant indicators used to assess an "individual microbial coefficient" due to potential individual variations.For a long time, our understanding of the holistic impact of microbial dysbiosis on human homeostatic equilibrium was limited.In light of this, we propose here a conceptual model (cell-microbe homoecology and co-homeostasis) elucidating why "microbial dysbiosis" influences "cellular homeostasis" (Fig. 6b).Building upon this model, commensal microbiota emerges as a additional regulatory force in maintaining homeostasis, in addition to the well-established roles of the nervous, immune, and metabolic systems.This foundational understanding lays groundwork for the establishment of a model to investigate the transformation between health and disease in the following discussion.

PHYSIOLOGICAL DEPENDENCE AND INTERNAL COMPETITION, HEALTH AND DISEASE
Moderate exposure of the human body to commensal microbiota is essential for maintaining the development and physiological functions of nervous, immune, and metabolic systems.The absence of commensal microbiota poses a potential risk to human health.However, to maintain healthy homeostasis, the body must continually counteract the potential damage caused by the dominant microbiota.While our preceding discourse included examples like Staphylococcus aureus and Candida albicans as conditional pathogens, it is imperative to recognize that, in a rigorous sense, all human microbes exhibit conditional pathogenicity.Essentially, real "mutualism" may not exist.

Controllable microbial community
Excessive proliferation of the microbiota at specific anatomical sites, such as small intestinal bacterial overgrowth (SIBO), can cause symptoms such as nausea, bloating, vomiting and abdominal pain, which may be caused by abnormalities in the structure or motility of the intestinal tract. 583In specific cases, the intervention of antibiotics also indirectly promotes the growth of specific microorganisms.For example, meropenem treatment reduced Clostridiaceae and promoted colonization and expansion of Bacillus polymorphus (BT) in the intestinal mucus layer. 584tact microbial barrier An intact barrier function is also a strategy to prevent microbiota translocation and its impact on distant tissues or organs. 5857][588] In mice with TET2 gene deficiency, microbial signals are key drivers of pre-leukemic myeloproliferation (PMP), inducing intestinal barrier dysfunction and systemic inflammation, particularly by increasing the production of interleukin-6 (IL-6). 589This development of PMP can be effectively reversed or prevented through antibiotic treatment and germ-free conditions. 589Additionally, mutations in the CRB1 gene compromise the barrier functions of retinal and colonic epithelial cells, leading to a disruption of critical intercellular junctions. 590Such impairment allows specific gut bacteria to translocate across the intestinal epithelial barrier, enter the bloodstream and eventually reach the retina, where they trigger a localized inflammatory response. 590This activation of immune cells causes retinal cell damage, culminating in retinal degeneration, and emphasizes the importance of an intact intestinal barrier in averting both systemic and localized pathological consequences. 590Other disease conditions, particularly diabetes and obesity, have been also associated with the isolation of bacteria from patients' adipose tissue. 591,592[595][596] Resist damage from microbial genetic mutations It is important to note that commensal microbiota exhibit "adaptive" properties to the humans across lifecycle stages.Different strains of microbiota colonizing the same host show different pathogenic characteristics.For example, the Enterococcus gallinarum strain in the intestinal lumen can be controlled by the host immune system, whereas the strain residing in the intestinal mucosal wall niche can translocate to the mesenteric lymph nodes and liver, causing inflammation that may be associated with specific gene mutations, changes in gene expression programs, and even the remodeling of cell wall structures. 597This similar divergent evolutionary pattern was also observed in Lactobacillus reuteri, suggesting that recognition of microbiota pathogenicity should be specific at the strain level. 597ducing exposure to harmful metabolites Although the human body can benefit from a variety of microbial products (as discussed above), harmful microbial products can also induce or exacerbate disease.Specifically, dietary substances such as choline, phosphatidylcholine (lecithin) and carnitine can be metabolized by the gut microbiota to trimethylamine (TMA).Physiological concentrations of TMA can damage tight junctions and increase permeability of the blood-brain barrier (BBB). 598][601] However, research has unveiled the intriguing potential of TMAO to augment the therapeutic efficacy of immunotherapy, particularly for the treatment of triple-negative breast cancer and pancreatic cancer. 602,603These findings underscore the importance of context-specific considerations when assessing the beneficial or deleterious impact of microbial products. 602,603lthough GF mice display anxiety-like behaviors (see discusstion in the section on the germ-free syndrome), certain gut bacteria strains, such as Bacteroides ovatus, metabolize dietary tyrosine into p-coumaric acid via the enzyme tyrosine ammonia lyase (encoded by BACOVA_01194). 604The p-coumaric acid is then converted to 4-vinylphenol (4VP) by phenolic acid decarboxylase, and subsequently reduced to 4-ethylphenol (4EP) by vinyl phenol reductase. 604The host's sulfotransferase SULT1A1 sulfates 4EP to produce 4-ethylphenyl sulfate (4EPS). 604Upon entering the brain, 4EPS induces changes in the activity and functional connectivity of specific brain regions, impairs the maturation of oligodendrocytes and reduces their interaction with neurons, can also leading to the manifestation of anxiety-like behaviors in the mice. 604In female patients with polycystic ovary syndrome, an increase in the gut microbiota Bacteroides vulgatus is associated with the characteristic manifestations of the syndrome, including excessive androgen levels, ovulatory dysfunction, and polycystic ovary morphology. 605On one hand, B. vulgatus, through its metabolic activities-particularly via the action of bile salt hydrolase enzymes-reduces the levels of glycodeoxycholic acid (GDCA) and tauroursodeoxycholic acid (TUDCA) in the gut.These bile acids are potent agonists of the farnesoid X receptor (FXR), and their decrease leads to weakened FXR signaling, which may in turn suppress the production of IL-22, a cytokine crucial for gut barrier and immune function, associated with the development of PCOS. 605On the other hand, agmatine produced by B. vulgatus from dietary arginine through the action of arginine decarboxylase acts as an endogenous agonist of FXR. 606The activation of FXR in intestinal L cells inhibits the expression of the proglucagon gene, which encodes the precursor of glucagon-like peptide-1 (GLP-1), decreased secretion of GLP-1 in response to glucose contributing to insulin resistance in PCOS. 607Similarly, Imidazole propionate (ImP) is a microbial metabolite produced from histidine that may regulate host inflammation to promote insulin resistance and is significantly elevated in the serum of diabetic patients. 608,609Three branched-chain amino acids (BCAAs), leucine, isoleucine and valine, synthesized by Prevotella copri and Bacteroides vulgatus, also increase the risk of diabetes. 610porA and fldH genes of the gut microbiota mediate the conversion of dietary phenylalanine to phenylacetic acid and phenylpropionic acid, respectively. 611The former can be synthesized into phenylacetylglutamine (PAGln), which enhances platelet activation and thrombogenic potential. 611In addition to metabolic molecules, microbial peptides can disrupt the body.For example, E. coli secretes ClpB, a melanocyte-stimulating hormone (α-MSH) analogue that can cause anxiety, anorexia and eating disorders. 612imilarly, the genus Bacteroides produces a myosin heavy chain 6 (MYH6) mimetic peptide, β-galactosidase, which can induce T-cell attack on the heart, causing fatal inflammatory cardiomyopathy. 613Recent research has identified several novel enzymes in the gut microbiota that have similar functions to those found in the host (Microbial-host-isozyme). 614Among these, the bacterial isoenzyme of the key diabetes target, dipeptidyl peptidase-4 (DPP4), can reduce the activity of endogenous GLP-1 in a mouse model of impaired intestinal barrier function which negatively affects glucose homeostasis. 614Notably, microorganisms can secrete exopolysaccharides (EPS) that cloak the LPS on their surface, which are typically recognized by the human immune system. 615By doing so, they diminish the activation of the hypothalamic acute stress response mediated by TLR4-TRPV1+ sensory neurons in the lungs, effectively sidestepping the body's defense mechanisms against infection. 615n summary, in the long-term co-evolution with microbes, both humans and microbes have developed various adaptive mechanisms that influence each other.Understanding human dependence and internal competition with commensal microbes is key to understanding the transition between health and disease, homeostasis and dysregulation (Fig. 7).It is known that coinhabitants can share 12% gut and 32% oral microbiota strains, so as a special point, certain non-communicable diseases such as cardiovascular diseases, diabetes, and inflammatory bowel diseases maybe predicted transmitted within human communities via human microbiota as intermediaries, becoming atypical infectious diseases. 616,617This gives rise to another concept: the social microbiome, which encapsulates the intricate interplay of microbial communities across a host's social fabric, shaping the landscape of health and disease. 618

CONCLUSION
The fusion of human sperm and egg creates our innate genome, while the microbiome, with its random and non-heritable nature, evolves as an adaptive genome.This adaptive genome is dynamic and personalized, constantly adapting to our physiology, pathology, environment, diet and microbial interactions.The innate genome and adaptive microbiomes are intertwined, resulting in the reprogramming of the organism's homeostasis.Loss of interaction with the adaptive genome is likely to result in germ-free syndromes (hypotheses based on germ-free animals).From a histological perspective, the human microbiota can be viewed as 'slave tissues' managed by the epithelial, connective, muscular and nervous tissues that have evolved from the inherent genome.The incorporation of slave tissue allows for an extension of the body's immune capabilities, providing an additional form of defence and immune modulation.When interacting with the external environment, understanding the host and its microbiome as a unified entity, or 'meta-host', may partially explain the heterogeneity in disease susceptibility, pathogenicity, severity and varying success rates of organ transplantation.When examining the internal relationship between the human body and its microbiota, it's understood that human tissues reap the potential benefits provided by the microbiome, while at the same time using various mechanisms to regulate and minimize the potential harms or costs associated with it.The homeostasis and dysbiosis of microorganisms with the human neural, metabolic and immune systems are the causal driving force behind health and disease outcomes.
Within the theoretical framework discussed above and diagrammatically presented in Fig. 8, the "germ-free syndrome" highlights the need to shift from the traditional view of "microbes as pathogens" to the understanding that "a lack of microbes can also be detrimental to health".The "Innate and adaptive genome" improves our understanding at the genetic and evolutionary level of the complete human genome, detailing the essential characteristics of the adaptive genome.The concept of "slave tissue" integrates ecological and human tissue perspectives, illustrating the intricate relationship between multicellular organisms and their associated microbiome.It elucidates how human master tissues can both reap benefits and endure adversities due to the presence of microbes.This concept redirects focus towards the alterations in 'slave tissue' as the disease progresses, emphasizing the dynamic interplay between host and microbe in health and disease.The "Acquired microbial immunity" unifies the roles of colonization resistance and immune regulation, considering the microbiome as a source of supplementary power to human defences.This concept provides a theoretical foundation for combating antibiotic misuse and for utilizing microecological therapies in the treatment of allergic and inflammatory diseases.The "Homeostasis reprogramming hypothesis" complements the foundations of modern medicine, represented by the "internal environment theory", by bridging the conceptual gap left by the neglect of the microbiome's role.This may in part explain the trend observed since the industrialization of a decline in some of the body's homeostatic indicators, such as basal body temperature and changes in blood glucose levels, in association with the body's microbial diversity.The "Cell-microbe co-ecology model" demonstrate the close association between "microbial regulation" and "cell homeostasis," offering a necessary understanding of why microbial dysregulation can impact homeostatic balance in humans.The "meta-host model" extends the definition of host.It suggests that symbiotic microorganisms act as co-hosts within the human ecological environment.The "Health-illness conversion model" elucidates the dual relationship between the innate and Fig. 7 The model of the interplay between the human innate and adaptive genome in health and disease transformation.The human innate and adaptive genomes form a holistic functional phenotype but are also in constant competition.The regulation of the nervous, immune, metabolic, and commensal microbiota constitutes the four major features and regulatory forces of human health and disease states.These forces interact with each other, and microbial dysbiosis can lead to the disruption of other forces and vice versa.The innate genome requires (a) the necessary exposure to commensal microbiota and a controllable microbial community, (b) an intact microbial barrier, (c) the ability to resist damage from microbial genetic mutations, and (d) the ability to utilize beneficial products of the adaptive genome and metabolize harmful ones to maintain a healthy steady state (with the innate genome in the dominant position).Conversely, (e) inadequate exposure to appropriate microbiota (which can lead to germ-free syndrome in extreme cases) or microbial overgrowth, (f) microbes or their components (e.g.LPS) entering the circulation through an incomplete barrier and causing harm to other tissues and organs, (g) microbial genetic mutations causing additional damage, and (h) a decrease in beneficial microbial products and an increase in harmful ones can lead humans towards disease progression (with the adaptive genome dominant).LPS Lipopolysaccharides, TMA Trimethylamine, TMAO Trimethylamine Noxide, PAGln Phenylacetylglutamine, ClpB a melanocyte-stimulating hormone (α-MSH) analogue, BCAAs Branched-chain amino acids, SCFAs Short-chain fatty acids, RKH Arginyl-lysyl-histidine adaptive genomes as a whole and their internal competition.It summarizes four patterns of microbial dysregulation within the human body.

FUTURE PERSPECTIVES
The recent release of the global burden report highlights the daunting challenges we face in various public health crises, including obesity and malnutrition, 619 cardiovascular diseases, 620 gastrointestinal disorders, 621 diabetes, 622 antimicrobial resistance 197 and cancers. 623The outbreak of the novel coronavirus has further compelled us to reflect on how we can enhance our prevention and treatment strategies for potential future infectious disease outbreaks. 624Microbiome, as the human adative genome, present a promising avenue for potential breakthroughs in this regard.Although progress has been made, the secrets of the relationship between humans and microbes have not been fully unlocked.More research is needed in the future to glimpse what lies beneath the tip of the iceberg.Some of the directions include but are not limited to the following: Protecting the diversity of human and environmental microbiomes, 625 avoiding the gradual loss of adaptive genomic elements, and establishing and maintaining microbiome banks are possible strategies that depend on interdisciplinary and international collaborations.These proactive measures have the potential to provide substantial benefits to diverse organisms, including augmented crop yields and bolstered resilience of plants in the face of climate change 626,627 and shows potential in protecting endangered animal species. 628urther deciphering the interaction mechanisms between the microbiota and other organs and tissues is essential.Currently, microbiota research on the following: The effects of other tissue developmental stages are insufficient; Viruses, 496,[629][630][631][632][633][634][635][636] fungi, 637,638 archaea [639][640][641][642] have received less attention than bacteria; Non-gut microbiomes are understudied; Fig. 8 A systematic framework for understanding human microbes and the history of the development of some of these concepts.The systematic framework consists of eight fundamental concepts/models: "innate genome and adaptive genome", "slave tissue", "acquired microbial immunity", "cell-microbe co-ecology and co-homeostasis model", "meta-host model", "health and illness transformation model" and "germ-free syndrome" Communication mechanisms between microbiomes from different sites, such as interaction between the gut and the lung/skin/oral, are not well understood; 4][645] These microbes promote tumor development by inducing mutations, affecting gene regulation, promoting inflammation, evading the immune system, and enhancing metastasis. 646Their interaction offers an additional opportunity for targeted cancer interventions; 647 Specific populations, such as rare disease patients, surgical patients, and transplant recipients, have not been well considered.
The causal relationship between microbes and diseases is still not well revealed.
The clinical applications of microbiomes mainly include diseases diagnosis (biomarkers), classification (severity), treatment (gene editing), and prognosis assessment.
Adaptive genomic elements and their effects on diet and responses must not be overlooked, as they have significant impacts on human physiology and therapy.Further characterization is required.
The utilization of "acquired microbial immunity" could offer additional therapeutic options for allergies, autoimmune diseases, and enteric infections, but potential risks should be carefully assessed with consideration of host conditions.
Standardized clinical guidelines are prerequisites for clinical translation."Microbial clinical specialists" and "microbial clinical department" are potential forms for future implementation.
The field of microbiome engineering is advancing with precision and complexity, employing a range of genetic strategies to manipulate the microbial ecosystem for therapeutic benefit. 648Engineered bacteria, such as E. coli Nissle 1917 strain, SYNB1020, effectively converts ammonia in the gut to L-arginine, ameliorating hyperammonemia and boosting survival rates in mice. 649By meticulously tuning key elements of gene expression, researchers have successfully achieved efficient biosynthesis of important compounds such as β-carotene and violacein in Saccharomyces boulardii. 650In an innovative approach to addressing C. difficile infections, researchers have developed a recombinant bacteriophage that expresses CRISPR RNAs to guide the native Cas3 protein in targeting and degrading the pathogen's chromosomal DNA, leading to the bacterial destruction. 651Programmable exogenous phage-delivered CRISPR/Cas9 delivery demonstrates the feasibility of strain-specific gene knockout and chromosomal deletion in complex microbial communities. 652For example, utilizing engineered M13 bacteriophages as vectors to specifically deliver the CRISPR-Cas9 system to E. coli within the mouse gut, enabling precise genetic editing at targeted loci despite the need to address challenges such as low bacteriophage viability and bacterial evasion of editing. 652Additionally, synthetic genetic elements developed through computational design enable the re-engineering of biosynthetic gene clusters for expression in various hosts. 653The innovative concept of microbial swarmbots encapsulates the synergy of multiple engineered microbes within microcapsules, working collectively to perform high-throughput functions. 654n the realm of microbiome research, equity is a critical issue. 655tudies from developing or impoverished nations are significantly disadvantaged and underrepresented compared to those from developed countries.In this regard, international professional associations, relevant governmental and societal research funding bodies, and academic journals should consider policy inclinations towards regions or research that are underrepresented.In areas or countries where it is challenging to organize large-scale population studies, the success of citizen science methods adopted by Belgium 118 and the recent proposal of the African Equitable Scheme by Ovokeraye H. Oduaran and colleagues are worthy of emulation. 656e are presently on the trajectory of comprehending natural phenomena, deciphering intricate mechanisms, and harnessing the potential of microbes to optimize human health.In the end, if it is truly possible for humans to colonize other planets, focusing merely on our innate genome while ignoring our adaptive genome could lead to wider health issues.Consequently, in all conceivable scenarios, contemplating an interplanetary microbiome initiative becomes an inevitable necessity.